Services

1. Biologic Filling 1/31/2012

   JHP has the Right Scale and Right Experience to meet a broad range of biologic filling needs.

2. Clinical Manufacturing In Viral Vaccines 4/14/2014

   Charles River offers more than 20 years of experience in manufacturing viral vaccines.

3. Sterile Injectable Contract Manufacturing 1/31/2012

   JHP Pharmaceuticals has both the Right Scale and Right Experience to meet a broad range of sterile injectable contract manufacturing needs.

4. Late Phase Regulatory Affairs 6/23/2011

   A multi-disciplinary and multi-lingual team of 25 Regulatory Affairs experts are at your disposal for all regulatory aspects of your Marketing Authorization Applications for Human and Veterinary Medicinal Products.

5. Biologics: From Molecule To Market 6/23/2011
   Developing a biologic therapy for market takes a special kind of expertise. SGS Life Science Services works with its clients to meet their specific needs in this complex field.
6. Regulatory Affairs Expertise 6/23/2011

   A multi-disciplinary and multi-lingual team of 25 Regulatory Affairs experts are at your disposal for all regulatory aspects of your Marketing Authorization Applications for Human and Veterinary Medicinal Products.

7. Therapeutic Areas 5/20/2011
   Deep therapeutic knowledge and understanding of the key issues combined with clinical development experience drives more effective and efficient pathways to commercialization.
8. Infectious Disease 5/20/2011
   We are facing an alarming increase of drug resistant microorganisms, global spread of infectious disease and the threat of bioterrorism and the development of antimicrobial agents is complex and expensive.
9. Phase I/IIa 5/17/2011
   You need to safely advance your drug candidate through phase I/IIa. The key to achieving this objective — on time — is to focus on maximizing critical data through strategic study design.
10. Product Safety And Pharmacovigilance

    A team of physicians, nurses, and pharmacists
    Throughout the life cycle of the program, Product Safety ensures timelines are met in global safety reporting in clinical trials, supports and educates site staff, and provides a safety profile through management and analysis of the safety data as part of their pharmacovigilance services. Our experienced, highly trained safety team is composed of physicians, registered nurses, clinical pharmacists, and medical technologists. These safety and surveillance experts specialize in the collection, evaluation, and submission of safety data in clinical trials. The cornerstone of all of the Product Safety services is the concise and rapid exchange of safety information among all parties.