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  Finished Product Development     Regulatory Affairs Consultancy     Active Pharmaceutical Ingredients (API) & Intermediates  
Jenson is working in partnership with reputable manufacturers and offering:

  • Supply of finished dosage forms
  • Supply of dossiers for finished dosage forms

  • Development and supply of finished dossier forms including API
More details...
Jenson can work with you in all stages of submission:

  • Before submission

  • During submission

  • After submission

For full information please visit JensonR+ website
Jenson can offer:
  • Market and patent evaluation

  • Sourcing and supply of generic APIs

  • Full GMP audit of API facility

  • Pre and Post Health Authority

  • Facility Inspection Support

  • Development of generic APIs
More details...
Adverse events should be reported. Reporting forms and information can be found at
Adverse events should also be reported to us on 01271 334 609 or
Please call 01271 334 609 for all medical enquiries.