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ALG

ALG

ALG is an international law firm based in Athens, Greece with lawyers qualified in 6 EU jurisdictions and Switzerland and is currently engaged by 25 biotech/pharma companies and 3 medical devices companies for their day-to-day contract drafting and negotiation. Services relate to drafting and negotiating several types of agreements to support operations in EMEA region, including drafting of best practice templates. Main characteristics are: quick turnaround for high volume-low risk contracts, expedited, efficient and solution oriented review of vendor comments in all types of agreements, multi-language capabilities of lawyers supporting the activity (English, French, German, Spanish, Italian, Portuguese, Romanian and Russian), excellent knowledge of the industry. In addition, it offers compliance support services, which consist of development and review of company’s compliance policies and SOPs, support on whistleblowing procedures, training on the pharmaceutical regulatory framework, review of marketing materials and advice on EU transparency disclosure requirements.
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ALG
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ALG
ALG is an international law firm based in Athens, Greece with lawyers qualified in 6 EU jurisdictions and Switzerland and is currently engaged by 25 biotech/pharma companies and 3 medical devices companies for their day-to-day contract drafting and negotiation. Services relate to drafting and negotiating several types of agreements to support operations in EMEA region, including drafting of best practice templates. Main characteristics are: quick turnaround for high volume-low risk contracts, expedited, efficient and solution oriented review of vendor comments in all types of agreements, multi-language capabilities of lawyers supporting the activity (English, French, German, Spanish, Italian, Portuguese, Romanian and Russian), excellent knowledge of the industry. In addition, it offers compliance support services, which consist of development and review of company’s compliance policies and SOPs, support on whistleblowing procedures, training on the pharmaceutical regulatory framework, review of marketing materials and advice on EU transparency disclosure requirements.
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