Acquisition / Placing

Advanced Medical Solutions Grp PLC 28 March 2002 For Immediate Release: 28 March 2002 Advanced Medical Solutions Group plc Proposed acquisition of MedLogic Global Holdings Limited ('MedLogic') and related intellectual property rights (the 'Acquisition') Proposed fundraising (the 'Fundraising') of 47,265,984 new ordinary shares of 5p each ('New Ordinary Shares') at 8.5p per share (the 'Issue Price') to raise £4.0 million Proposed capital reorganisation Transfer from the Official List to AIM Winsford, Cheshire: Advanced Medical Solutions ('AMS' or the 'Company') today announces that it has conditionally agreed to acquire MedLogic, the holding company of a UK based group specialising in the development and manufacture of medical grade adhesives for the wound closure market, and related intellectual property rights for a consideration of US$3.5 million (£2.5 million). AMS also announces the Fundraising to finance the Acquisition and ongoing working capital requirements of MedLogic. The Fundraising, consisting of a placing with venture capital trusts and other investors (the 'VCT Placing') and a placing subject to clawback by existing shareholders (the 'Placing and Open Offer'), will raise, in total, £4.0 million. To facilitate the Fundraising, it is also proposed that a reorganisation of the Company's share capital be implemented and that the Company's listing be transferred from the Official List of the UK Listing Authority to the Alternative Investment Market of the London Stock Exchange ('AIM'). AMS' preliminary audited results for the year ended 31 December 2001 were also announced this morning and were in line with market expectations. Highlights: • Proposed $3.5 million (£2.5 million) acquisition of MedLogic and related intellectual property rights • Issue of 47,265,984 New Ordinary Shares at 8.5p per share to raise £4.0 million • Proposed capital reorganisation • Transfer from the Official List to AIM • Preliminary results announced today in line with market expectations Commenting on the Acquisition and Fundraising, Dr. Geoffrey Vernon, Chairman of AMS said: 'Following the strengthening of the underlying business seen over the last few years, the Board believes that AMS' core woundcare operations have been developed to a point where it has become appropriate to seek synergistic external opportunities to accelerate growth and enhance shareholder value. It is our belief that the Acquisition represents an exciting opportunity for the Group to develop critical mass as a medical device company. 'Break-even should still be achieved in line with market expectations - indeed we are confident that the Acquisition should transform the prospects of AMS by accelerating growth in revenues and earnings beyond what can be achieved by organic growth alone. We also hope to benefit from synergies between the two companies - synergies that will allow AMS to leverage its existing relationships with its partners whilst using MedLogic's direct sales force to cross sell AMS' wound dressings.' For further information please contact: Advanced Medical Solutions Group plc On 28.03.02: +44 (0) 20 7466 5000 Don Evans, Chief Executive Thereafter: +44 (0) 1606 863 500 Mary Tavener, Finance Director www.admedsol.com Robert W. Baird Limited Tel: +44 (0) 20 7488 1212 Shaun Dobson Buchanan Communications Tel: +44 (0) 20 7466 5000 Nicola How / Fergus Mellon This announcement has been approved by Robert W. Baird Limited for the purposes of Section 21 of the Financial Services and Markets Act 2000. Robert W. Baird Limited, which is regulated by the Financial Services Authority, is acting as the Company's financial advisor and stock broker in connection with the proposed Fundraising. Overview: AMS has conditionally agreed to acquire the issued share capital of MedLogic, the holding company of MedLogic Global Limited ('MedLogic Global' and together with MedLogic the 'MedLogic Group'), a UK based company specialising in the development and manufacture of medical grade adhesives for the wound closure market, and associated intellectual property rights ('IPR') from The Travelers Insurance Company Inc. for a consideration of $3.5 million (£2.5 million). The consideration is payable as to $3.3 million (£2.3 million) in cash on completion and by the issue of 1,263,158 new ordinary shares ('the Consideration Shares'). The cash consideration is subject to a retention of $425,000 (£297,828). In addition, to finance the Acquisition and additional working capital, the board of AMS (the 'Directors' or the 'Board') announces the VCT Placing and the Placing and Open Offer to raise approximately £4.0 million by way of the issue of 47,265,984 New Ordinary Shares at a price of 8.5p per New Ordinary Share. The Acquisition, the VCT Placing and the Placing and Open Offer are conditional upon, inter alia, the receipt of provisional assurances from the Inland Revenue that the shares subject to the VCT Placing ('VCT Shares') will qualify for investment by Venture Capital Trusts and will be eligible for relief under the Enterprise Investment Scheme and the passing of certain Resolutions to be proposed at an extraordinary general meeting of the Company convened for 23 April 2002 ('the EGM'). Pursuant to an agreement ('the Placing and Open Offer Agreement'), Robert W. Baird Limited ('Baird') has conditionally agreed to place the New Ordinary Shares with institutional and other investors. The VCT Shares are being placed firm and the shares placed in the Placing and Open Offer (the 'Open Offer Shares ') are being placed subject to clawback by Qualifying Shareholders under the Open Offer. The VCT Placing and the Placing and Open Offer have been fully underwritten by Baird. As at the close of business on 27 March 2002, the price of an Existing Ordinary Share, as derived from the Official List, was 9.5p, which is below its nominal value of 10p. In order to facilitate the VCT Placing and the Placing and Open Offer, the Board is proposing the Capital Reorganisation, pursuant to which each Existing Ordinary Share will be sub-divided and converted into one Ordinary Share of 5p ('Reduced Ordinary Share') and one non-voting deferred share of 5p ('Deferred Share') subject to approval at the EGM. The Capital Reorganisation will not affect Shareholders' relative rights in the share capital of the Company. The Board also considers that, due to the size of the Company and the ability of AIM companies to attract investment from Venture Capital Trusts, the Company should move from the Official List and apply for its shares to be admitted to trading on AIM. The Company hereby gives notice of the intended cancellation of the listing of the Existing Ordinary Shares on the Official List and of admission to trading of the Existing Ordinary Shares on the London Stock Exchange at the close of business on 29 April 2002. Application has been made to the London Stock Exchange for the admission of the Reduced Ordinary Shares, the New Ordinary Shares and the Consideration Shares to trading on AIM. AMS: Introduction The AMS business was established in 1991, primarily to utilise proprietary polymer technology in the development of a new generation of advanced wound dressings which addressed the growing acceptance by medical professionals of the concept of 'moist healing' - keeping a wound moist during the healing process rather than, as was traditional, exposing it to the air - which has been shown to reduce scarring and accelerate healing. AMS has since developed a range of advanced wound dressings designed to manage wound fluids and maintain optimal levels of moisture to promote healing. The acquisition of related technologies and the incorporation of a wide range of materials such as alginate, film, foam, gel and hydrocolloids, has resulted in AMS' product portfolio covering the full spectrum of wounds, from cuts and grazes, to heavily exuding and bleeding wounds through to dry wounds such as burns. Strategy Since January 2000, when the current executive management team was formed, the focus of the AMS Group has been on achieving profitability from its core woundcare business within existing cash resources and building a solid financial platform from which to grow a leading medical device company. As part of this strategy AMS has established strategic partnerships with blue chip companies, such as Smith & Nephew, 3M, Johnson & Johnson, Novartis and Coloplast. These partnerships will allow the Company to bring new products and technology to global markets in a timely fashion. The Directors believe that these relationships coupled with the Company's manufacturing expertise and technology pipeline form the basis for future growth and sustainable profitability for the AMS Group. The MedLogic Group: Introduction MedLogic Global, the trading subsidiary of MedLogic, develops, manufactures and markets medical grade adhesives and sealants principally for topical wound closure and wound management. The wound closure products are designed to replace or supplement alternative methods of closure such as sutures, staples or adhesive strips. The sealants are intended to protect skin from infection and break-down due to friction, shear or the presence of moisture. MedLogic Global Corporation ('MGC'), the parent company of MedLogic, was established in Colorado Springs, Colorado, United States, in 1991 where the initial development of the MedLogic Group's product portfolio was undertaken. In 1997, MGC acquired a medical device manufacturing facility in Plymouth, UK and established the MedLogic Group in the UK. Subsequently, all of MGC's operations were consolidated onto the Plymouth site. MGC no longer has any US based trading operations. Its two key assets, the share capital of MedLogic, the holding company of MedLogic Global, and the IPR portfolio relating to the MedLogic Group's business, are being acquired by AMS. Technology Overview MGC developed its technology platform and IPR portfolio based on the optimisation and commercialisation of cyanoacrylate adhesive materials (commonly known as superglues), specifically n-butyl cyanoacrylate - an advanced version of the base material offering characteristics more favourable for clinical applications. Cyanoacrylates were originally developed in the 1950s and the fundamental patents covering their use as basic tissue adhesives have already expired. MGC and MedLogic Global have pursued a strategy of developing special methods of use and protecting improvements made to the core formulation which enhance its performance as a wound closure or wound management material. In total, MGC has 76 patents either issued or pending. For each of its products, MGC and the MedLogic Group has developed a unique and proprietary formulation of n-butyl cyanoacrylate, plasticisers (for flexibility) and inhibitors (for setting rate) to deliver a specific end product with suitable properties for its given application. The addition of specific anti-microbial compounds into the formulation of its wound sealant products without adversely affecting their properties is considered by the Directors to be a significant technological breakthrough that would enhance the current product range. MGC and MedLogic Global have a number of patents covering the use of anti-microbial agents in cyanoacrylates. In addition, MGC has patented the use of low dose electron beams for the sterilisation of its formulations. This has advantages over alternative methods of sterilisation, such as heat or gamma radiation, as it is not as detrimental to the material properties of the compound, requires the incorporation of fewer stabilisers, allows for a longer 'shelf life' and is relatively cost effective. The Directors believe that the patented electron beam sterilisation capability is an important ongoing competitive advantage for MedLogic Global. MGC also has a portfolio of hydrogel patents, acquired in 1998, that covers materials that are influenced by body temperature such that they provide the potential for the delivery of 'active' ingredients. The Directors believe that some of these patents, when combined with AMS' own hydrogel technology, could have significant potential to advance the Enlarged Group's work on 'active' tissue repair. The IPR relating to all of the above technology is being acquired by AMS as part of the Acquisition. Products and markets The n-butyl cyanoacrylate technology developed by MGC and MedLogic Global provides a platform for entry into multiple healthcare markets. Specific products have been developed to address a number of these markets and a number of further products are in development. MedLogic Global's current active portfolio consists of two products: • LiquiBand(R) - a tissue adhesive for wound closure. • LiquiShield(R) (SuperSkin(R)) - a tissue barrier film for wound management. These products are detailed below: LiquiBand(R) - Wound closure The world-wide wound closure market is widely estimated to be approximately US$3.3 billion (£2.3 billion) at retail prices. The market consists of four distinct segments: • Sutures: the use of needle and thread. • Staples: the use of metallic devices to hold the tissue edges together during healing. • Adhesive strips: the use of small pieces of tape, often 'butterfly' shaped. • Tissue adhesives: the 'glueing' together of the edges of wounds. Tissue adhesives are a comparatively recent introduction and currently account for a relatively small but growing proportion of the market. It is generally estimated that as much as 40 per cent. of the global suture and staple market could eventually be accounted for by tissue adhesives and sealants. The perceived advantages of tissue adhesives over alternative methods include: • ease and speed of application; • reduced patient trauma (no anaesthetic or needles required); • superior wound sealing; • reduced infection potential; • improved cosmetic outcome; and • relatively low total treatment costs. The Directors believe that tissue adhesives will account for an increasing share of the wound closure market, replacing adhesive strips, sutures and staples, as recognition of their competitive advantages within the healthcare environment increases. LiquiBand(R) is MedLogic Global's disposable, single-use liquid adhesive device designed to close and seal the epidermal layer of a wide variety of traumatic and surgical wounds. MedLogic Global obtained a Class 2A device CE mark for LiquiBand(R) in the European Union in June 1998 and began commercialisation of the product in 1999, focusing on selling to Accident and Emergency ('A&E') units in the UK, where it is listed on the Drug Tariff. MedLogic Global has its own direct sales force to access the A&E market and also plans to distribute via NHS Logistics, the centralised supplier for the National Health Service. The LiquiBand(R) product has enjoyed widespread acceptance in the UK A&E unit market selling into almost 50 per cent. of hospitals. LiquiBand(R) has three key competitors in the UK: Dermabond (Closure Medical); Indermil (Tyco); and Histacryl (Braun Aesculap). The Directors believe that LiquiBand(R) has a number of competitive advantages over its competitor's products, in terms of its physical properties and ease of use, and that these advantages have resulted in a wider acceptance of the LiquiBand(R) product. A comparative study of Indermil, Dermabond and LiquiBand(R) carried out by the School of Nursing and Midwifery at the University of Sheffield in October 2000, concluded that 'the LiquiBand(R) tissue adhesive produced the most consistent results, scoring higher on most categories when compared with the other tissue adhesives'. MedLogic Global has recently commenced the appointment of distributors in certain European countries to promote and sell LiquiBand(R) in these markets. The Directors believe that the Dermabond product from Closure Medical (which is marketed by the Ethicon division of Johnson & Johnson) has by far the major share of the global tissue adhesives market as it is the only tissue adhesive to be approved for sale in the USA as of March 2002. The Directors believe that the successful sales and rapid growth of Dermabond in the USA demonstrate the potential for the tissue adhesive market and that this success will attract other major international woundcare players to this segment of the wound closure market. It is the intention of the Directors to progress the regulatory approval process required for LiquiBand(R) to enter the US market in due course. LiquiShield(R) - Wound management Wound management products range from traditional gauzes and adhesive plasters to the advanced moist woundcare dressings as currently sold by AMS. The use of medical adhesives as a barrier for the protection of skin is a relatively new concept. LiquiShield(R) is a topical, liquid barrier film that is painted onto the skin in a very thin layer in order to provide protection against skin damage caused by friction, shear and/or the presence of moisture which can lead to skin breakdown, particularly in radiation patients, amputees utilising prosthetic limbs, stoma patients, bedridden patients, paraplegics, quadraplegics and individuals with generally compromised skin integrity. LiquiShield(R) has potential applications in each of these areas. LiquiShield(R) (original name SuperSkin(R)) was MedLogic Global's first commercial product. It received FDA clearance for sale in the USA in December 1997 and a CE mark for sales into Europe in April 1998. While it was renamed LiquiShield(R) for the US market, it continues to be sold under the name of SuperSkin(R) in the UK. LiquiShield(R) is sold through distributors in the USA and Europe, targeted mainly at the nursing home sector. The Directors believe that the formulation of the Liquishield(R) product provides a number of competitive advantages. Future developments Future developments of the MedLogic Global product range will be aimed at improving delivery systems to make the products easier to use, enhancing formulations to achieve specific product properties for new markets and incorporating anti-microbial agents into the products. Products currently in development include: LiquiBand Surgical(R) - a product designed specifically to take the LiquiBand(R) product into operating theatres and thus expand its potential use within hospitals. An enhanced formulation of the cyanoacrylate makes this product suitable for closing surgical incisions in the sterile environment of the operating theatre. The Directors believe that this product will be ready for launch in during 2002. LiquiDrape(R) - a cyanoacrylate sealant designed to replace surgical incise drapes (sterile films that are applied to the skin prior to surgical incision to protect the wound from local infection) and enhance infection control at the site of a surgical incision. Incise drapes are used in procedures where a higher than normal risk of infection exists and are only used on relatively flat or uniform skin surfaces, as they are extremely difficult to apply over joints or variable skin surfaces. LiquiDrape(R), a thin-film, liquid barrier, addresses this application problem as it is painted onto the operative site after it has been prepped. This product will be undergoing regulatory approval and the Directors believe it can be launched into selected European markets by the end of 2002. Financial information The MedLogic Group recorded its first sales in January 1999 and overall sales have grown significantly since that time. The majority of turnover during the period was earned from the LiquiBand(R) product as it became more widely accepted in A&E units in the UK. In order to establish products in their market places and to rapidly grow sales, the MedLogic Group sacrificed short-term profitability. Net losses in the periods to 30 June 1999, 2000 and 2001 were £1.6 million, £1.7 million and £1.0 million respectively. Much of these losses related to the sales and marketing function and the establishment of the product distribution channels. Net liabilities as at 30 June 2001 were £4.7 million. The MedLogic Group has been financed to date by intercompany loans from MGC which are excluded from the Acquisition. As at 30 June 2001 the balance of these loans was £5.0 million. The Acquisition: Principal terms AMS has conditionally agreed to purchase the entire issued share capital of MedLogic together with related IPR. The $3.5 million (£2.5 million) consideration payable by the Company for the Acquisition is to be satisfied by the payment of $3.3 million (£2.3 million) in cash and by the issue of the Consideration Shares. $425,000 (£297,828) of the cash consideration is to be retained in an escrow account for a period of one year from completion of the Acquisition Agreement to provide security in the event of certain claims by AMS under the Acquisition Agreement. Usual warranties and indemnities for a transaction of this nature have been given by MGC to AMS, its obligations being guaranteed in this regard by Travelers. The Acquisition Agreement is conditional upon, inter alia, the following: - Shareholders passing the ordinary resolution to be proposed at the EGM; and - Admission of the Open Offer Shares and the Consideration Shares to trading on AIM. Background to, and reasons for, the Acquisition and the Fundraising The Board believes that the AMS Group's core woundcare operations have been developed to a point where it has become appropriate to seek synergistic external opportunities to accelerate growth and enhance Shareholder value. In evaluating selective acquisition opportunities the Board has used the following criteria: • they should be a strong strategic fit with AMS' existing businesses; • they should move the AMS Group into higher value products; • they should leverage the AMS Group's current capabilities; and • they should not delay break-even for the existing AMS businesses. The Board is of the opinion that the Acquisition satisfies all of the above criteria and, as such, represents a significant opportunity to develop a larger, more attractive medical devices group. The complementary nature of the MedLogic Group's product portfolio and technologies significantly increases the markets available to the Enlarged Group and assists in positioning the Enlarged Group into the 'higher end' tissue repair sector of the wound care market segment. The Directors also believe that the Acquisition enables the Enlarged Group to: • leverage existing distribution channels: - utilise AMS' blue-chip partners to offer new outlets for the MedLogic product range, and - utilise MedLogic's direct sales force in the UK to cross sell AMS' wound dressings into A&E units; • leverage senior management and overheads in research and development, sales and marketing, finance and logistics. The Directors believe that the Acquisition represents an exciting opportunity for the Enlarged Group to develop critical mass as a medical device company. They are confident that the Acquisition will not delay the AMS Group achieving break-even in line with current market expectations and believe that the Acquisition could transform the prospects of AMS by accelerating growth in revenues and earnings beyond what can be achieved by organic growth alone. The Company is proposing to raise £4.0 million by way of the VCT Placing and the Placing and Open Offer to finance the cash consideration of the Acquisition, the expenses of the VCT Placing, the Placing and Open Offer, the Capital Reorganisation and the Acquisition and to provide additional working capital for the MedLogic Group. The Directors believe that undertaking the VCT Placing and the Placing and Open Offer will allow AMS to maintain cash headroom for the ongoing development of the AMS Group's businesses and ensure that the financial integrity of the Enlarged Group is not compromised. The transfer to AIM and the Capital Reorganisation are being proposed to facilitate the VCT Placing and the Placing and Open Offer. Transfer to AIM Following consultations with the Company's major Shareholders, the Board has decided that it is in the best interests of the Company and Shareholders for trading in the Company's shares to be transferred to AIM. The AIM Rules require that the Company appoints a nominated adviser and broker before its Reduced Ordinary Shares are admitted to trading on AIM. Robert W. Baird Limited has agreed to act as nominated adviser and broker to the Company. Current trading and prospects The Company today announced its audited results for the year ended 31 December 2001 which showed good progress towards its goal of achieving profitability within its existing cash resources. Since 30 June 2001, the date to which the latest audited financial statements of MedLogic were prepared, MedLogic Global has experienced further growth in sales on an annualised basis. The majority of this growth has been generated by increased sales of the LiquiBand(R) product. The Directors believe that this has been driven by both an increase in the number of customers, and higher average volumes per customer as the product has gained wider acceptance and utilisation for wound closure within UK A&E units. Gross profits have continued to improve as volumes through the Plymouth facility have increased. The facility, which is certified to ISO 9001 and EN 46001 standards and is designed to operate in accordance with the US FDA's Quality System Regulations, has the capacity to allow for further significant sales growth. In overall terms, gross margin has decreased principally because monomer, previously manufactured by MGC, is being sourced from third parties. This has resulted in a loss making distribution contract for LiquiShield(R) which may require renegotiation. MedLogic continues to generate losses at the operating level which have increased its balance sheet debt and required further funding from MGC. Following the Acquisition, the market available to the Enlarged Group will increase significantly by the addition of the rapidly expanding tissue adhesive segment of the wound care market. This will move the Enlarged Group to higher value business and re-enforce its image as a tissue repair company rather than a contract manufacturer of 'dressings'. AMS' established capability in partnering with blue-chip companies will be utilised to move the MedLogic product range into global markets. Additionally, key AMS products used for treating and dressing wounds will be sold into UK A&E departments by the MedLogic direct sales team. The Directors believe that these synergies, together with operational efficiencies in overhead functions, will allow revenue and earnings growth of the Enlarged Group to be accelerated over and above that of the core AMS business. As a result, they are optimistic about the Enlarged Group's future prospects. Details of the VCT Placing and the Placing and Open Offer The Company is proposing to raise approximately £4.0 million pursuant to the VCT Placing and the Placing and Open Offer by the issue of 47,265,984 New Ordinary Shares at the Issue Price. Baird, as agent for the Company, has conditionally agreed to place the VCT Shares and the Open Offer Shares at the Issue Price with institutional and other investors or failing which itself to subscribe for the New Ordinary Shares. The Open Offer Shares are subject to clawback to satisfy valid applications by Qualifying Shareholders under the Open Offer. The VCT Shares have been placed firm with certain institutional and other investors and venture capital trusts and are not subject to clawback under the Open Offer. All of the Directors have irrevocably undertaken to the Company and Baird to take up their full entitlements of Open Offer Shares under the Open Offer. In addition to their full entitlements under the Open Offer and subject to compliance with the provisions of the model code of the Listing Rules, certain of the Directors also intend to subscribe for an aggregate of 516,410 VCT Shares. Baird, as agent for the Company, will make the Open Offer under which Qualifying Shareholders are being given the opportunity to subscribe for Open Offer Shares at 8.5 p per share on the following basis: 8 Open Offer Shares for every 35 Existing ordinary Shares held by them at the close of business on 22 March 2002 (the 'Record Date') and so on in proportion for any number of Existing Ordinary Shares then held. Fractions of Open Offer Shares will not be allotted to Qualifying Shareholders but, together with Open Offer Shares attributable to those overseas shareholders that are not eligible to participate in the Open Offer, will be aggregated and subscribers will be procured for them under the Placing and Open Offer Agreement and the proceeds will be retained for the benefit of the Company. Qualifying Shareholders may apply for any number of Open Offer Shares up to their maximum entitlement, as set out in their Application Form. Qualifying Shareholders should be aware that the Open Offer is not a rights issue and that Open Offer Shares not applied for under the Open Offer will not be sold in the market or otherwise for the benefit of those who do not apply under the Open Offer. Completed application forms under the Open Offer must be received no later than 3.00 pm on 23 April 2002. The latest time and date for splitting application forms (to satisfy bona fide market claims only) is 3.00 pm on 19 April 2002. Application forms are personal to the Qualifying Shareholders named thereon and are transferable only to satisfy bona fide market claims. The Open Offer Shares and the VCT Shares will, when issued, rank pari passu in all respects with the Reduced Ordinary Shares. Capital Reorganisation At the close of business on 27 March 2002, the price of an Existing Ordinary Share, as derived from the Official List was 9.5p which is below its nominal value of 10p. Pursuant to the Companies Act, a company is prohibited from issuing shares at a price below their nominal value and therefore, in order to facilitate the VCT Placing and the Placing and Open Offer, it is proposed that the Capital Reorganisation be implemented. Pursuant to the Capital Reorganisation, each Existing Ordinary Share with a nominal value of 10p will be subdivided into one Reduced Ordinary Share and one Deferred Share, each with a nominal value of 5p. Each unissued Existing Ordinary Shares of 10p will be sub-divided into two Ordinary Shares of 5p each. Each Reduced Ordinary Share will, after allowing for the effect of the Capital Reorganisation, carry the same rights including voting, dividend and capital repayment rights as an Existing Ordinary Share. Each Deferred Share will carry no voting rights, will not rank for dividends and will only participate on a winding up of the Company after the sum of £1,000,000 has been paid in respect of each Reduced Ordinary Share. No listing or quotation on any stock exchange will be sought for the Deferred Shares and no share certificates will be issued. The value of a Deferred Share will therefore be minimal and the value of the Existing Ordinary Shares will be reflected in the Reduced Ordinary Shares. The Capital Reorganisation will have no effect on the Group's net assets and will not affect the value of each Shareholder's investment in the Company. General A prospectus, to be dated 28 March 2002, (the 'Prospectus') containing details of inter alia, the Acquisition, the VCT Placing and the Placing and Open Offer and notice of an Extraordinary General Meeting, convened for 11.00 am on 23 April 2002 to be held at the Blue Cap, 520 Chester Road, Sandway, Northwich, Chesire, CW8 2DN, will be posted to shareholders later today, together with an application form for use in connection with the Open Offer and a form of proxy. Copies of the Prospectus will be available to the public free of charge from the offices of Robert W. Baird Limited, Mint House, 77 Mansell Street, London E1 8AF from today until a period of not less than 14 days after the date that dealings commence in the New Ordinary Shares. Expected Timetable of Principal Events 2002 Record Date for the Open Offer close of business on 22 March Latest time and date for splitting of Application Forms (to satisfy bona fide market claims in relation to Existing Ordinary Shares) 3.00 p.m. on 19 April Latest time and date for receipt of Forms of Proxy 11.00 a.m. on 21 April Extraordinary General Meeting 11.00 a.m. on 23 April Latest time and date for receipt of completed Application Forms and payment in full under the Open Offer 3.00 p.m. on 23 April Record date for Capital Reorganisation 29 April Existing Ordinary Shares de-listed from the Official List close of business on 29 April Dealings in the Reduced Ordinary Shares commence on AIM 30 April Dealings in the VCT Shares commence on AIM 30 April CREST stock accounts credited with VCT Shares 30 April Completion of the Acquisition, dealings in the Open Offer Shares and the Consideration Shares commence on AIM 1 May CREST stock accounts credited with Open Offer Shares 1 May Despatch of definitive share certificates for the Reduced Ordinary Shares, the VCT Shares and the Open Offer Shares and the Consideration Shares where applicable 7 May Amounts expressed in US dollars have been translated into Sterling at a rate of US $1.427 = £1 This information is provided by RNS The company news service from the London Stock Exchange
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