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GPP Consulting Group Introduction      / Product      Contact
  Tailor made process optimisations

GPP has found its ideological background by the philosophy of GMP/GDP known by the pharmaceutical industry years ago.

In our efforts to make
  - Solid structuring
  - Logic planning processes (planograms)
  - Constant drive for simlicity
  - Transparency
  - Efficient purchase & delivery controls with SAP
we develop consistent study proposals & projects to implement.


„We are a multi culturel bunch of qualified employees with a globally
active network. Eager to provide – added value – and make so our daily
work a bit more fun.“


New Partnership with Interactive Consulting Associates GmbH - Daniel Fischer

We are very pleased to announce a new GMP Auditor relation with Interactive Consulting Associates GmbH, Switzerland.

Their experts cover all aspects of GMP for APIs and limited the GMP aspects of final dosage forms.


Strategic Dialogue

GPP attempts to create solutions which will lead clients to successful, measurable solutions. Consequently, the customer invests a maximum time of 6 weeks for the preliminary study, which is generally free of charge, and will get afterwards a ready table of project specific details.


„In all work we do what it likes to be apreciated and honoured. Applaus is our kick.“





GPP - Tool

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At each level of a project,
whether it be:

  - Research
  - Development
  - Registration
  - Manufacturing of dosage form
  - Cost opimised manufacture

GPP offers vital expertise. The essential
basic for clients business success.
More rapid introduction (launch) into
the market.


„Clients profit of an ingenious, unique and
clever designed consutation-pyramid.“
  • Update of old dossiers/licences
  • Joint development
    • API manufacturers
    • Generic drug manufacturers working in non-regulated makets in accordance with cGMP requirements
  • Focus on sourcing
  • Generic drug manufacturers with a local focus
    • Outlicensing
    • Export
  • Regulatory affairs service
    • Concept as to how we wish to offer that in the future
  • Group internal logistics company (FGS)
    • Cost-oriented transport
    • Dangerous goods specialists (IATA, ADR/RID, IMO/IMDG)
  • Expert handling in the dispatch of drugs in dosage form
  • Assessment of licensing opportunities
  • Analysis of documentation weaknesses
  • Literature research using in-house and external databases
  • Specialist reports
  • Dossier compilation
  • Drafting of licensing documentation in Common Technical Document (CTD) format, ready for submission
  • Responsibility for licensing procedures in all EU countries/MRP and central procedure
  • Reformatting of old documentation into the CTD format
  • Compilation of Investigational Medicinal Product Dossiers (IMPD)
  • Consultation on issues relating to the Medicines Act (Arzneimittelgesetz)
  • Processing of all regulatory procedures with national authorities
  • Preparation of official texts in accordance with national legal requirements
  • Validations
  • Competent internal and external contact partners
  • Arranging and provision of examined and EU/conforming registration dossiers
  • Generic drug manufacturers with a local focus
    • Outlicensing
    • Export
  • Regulatory affairs service
We offer you:
  • Alternatives to conventional or recognised sources
  • Choice of the ideal manufacturer:
    • Price
    • Quality
    • Documentation
  • Exclusivity agreements
  • Framework and supply agreements over fixed periods
  • Customer-specific patent clarifications and product development strategies in the respective area of indications
  • Subsidiary companies and local branches in Poland, India, Korea and China
  • Rapid delivery due to efficient processes with local authorities
    • Narcotics licence
    • Inspection (e.g.SGS)
    • Attestations
  • Group internal logistics company (FGS)
    • Cost-oriented transport
    • Dangerous goods specialists (IATA, ADR/RID, IMO/IMDG)
  • Efficient purchase and delivery controls thanks to SAP
We offer you:
  • Outsourcing of processes including synthesis and process optimisations
  • Market research for support with Make-or-Buy decisions
  • Optimisation of difficult and expensive cleaning measures
  • Development of tailor-made new “advanced intermediates”
  • Subsidiary companies and local branches in Poland, India, Korea and China
  • Rapid delivery as a result of efficient processes with local authorities
    • Inspection
    • Attestations etc.
  • Group internal logistics company (FGS)
    • Cost-oriented transport
    • Dangerous goods specialists (IATA, ADR/RID, IMO/IMDG)
  • Efficient purchase and delivery controls thanks to SAP
We offer you:
  • Assessment of licensing opportunities
  • Analysis of documentation weaknesses
  • Literature research using in-house and external databases
  • Specialist reports
  • Dossier compilation
  • Drafting of licensing documentation in Common Technical Document (CTD) format, ready for submission
  • Responsibility for licensing procedures in all EU countries/MRP and central procedure
  • Compilation of Investigational Medicinal Product Dossiers (IMPD)
  • Consultation on issues relating to the Medicines Act (Arzneimittelgesetz)
  • Processing of all regulatory procedures with national authorities
  • Preparation of official texts in accordance with national legal requirements
  • Competent internal and external contact partners
We offer you:
  • Generic drug manufacturers with a local focus
    • Outlicensing
    • Export
  • Regulatory affairs service