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Sourcing Inquiry Logo Phagecon

Phagecon

Regions
Europe, Worldwide
Countries
Portugal, Cyprus, …
Countries
Portugal, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Macedonia, Malta, Montenegro, Mozambique, Netherlands, Poland, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, United Kingdom, Angola, Austria, Belgium, Brazil, Bulgaria, Cape Verde, Croatia
Size
20-50
Specialty
Human Medicines, Biopharmaceuticals, …
Specialty
Human Medicines, Biopharmaceuticals, Generics, Animal Medicines, Cosmeceuticals, Nutraceuticals, Medical Devices
Service category
Pharmaceutical process development and validation, GMP audit services, …
Service category
Pharmaceutical process development and validation, GMP audit services, Quality management services, Certification services, Regulatory services - CMC writing - medical writing, Pharmacovigilance and QPPV services, Consulting - strategy and development, Legal counselling, Translation services (medical, clinical, pharmaceutical), Marketing, Sales, PR and communication, Training and education, Partnering/collaboration for drug dossiers, patents, drug candidates, medical technology, Others
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Summary

PHAGECON - Pharmaceutical Services and Consulting, Ltd. is dedicated to providing quality services to the Pharmaceutical Industry across all Europe.
We present a wide range of services in Regulatory Affairs, Pharmacovigilance, Medical/Scientific and Pharmaceutical Affairs enabling us to follow the life cycle of companies and their health products.

Our experience and operational flexibility allow us to offer our customers an overall and customised solution to any request related to regulatory, technical and scientific affairs.

Phagecon’s senior managers have work experience at National Agencies / Authorities and in the Pharmaceutical Industry holding solid expertise in activities such as:

  • Assessment of scientific data;
  • Centralised, decentralised, mutual recognition and national procedures;
  • Clinical trial applications; Compiling/writing of dossiers;
  • Classification of drugs, medical devices, cosmetics and food supplements;
  • eCTD compilation and publishing;
  • GMP and GDP audits;
  • Readability/user testing;
  • Liaison with authorities;
  • Licensing;
  • Medical writing;
  • Pharmacovigilance;
  • Pricing&Reimbursement;
  • Promotional material review;
  • Readability User Testing;
  • Renewals;
  • Regulatory intelligence and strategy;
  • Trainning;
  • Translations;
  • Variations;
  • Writing of summaries and expert reports,
  • among many others.

Our partners & customers have a competitive advantage over their competitors: they have the guarantee that all services hired will be carried out successfully, on time and will bring added value to their organisations!

 

Specialties

Regulatory affairs, Pharmacovigilance, Medical & Scientific Affairs, Pharmaceutical Affairs (QMS, GMP, GDP), Regulatory Submissions, Strategic Planning, Project management, European coverage, Market Access, Medical writting, Readability User Testing

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