ANYTHING A PERSON CAN IMAGINE, THEY CAN ACHIEVE!
The tpi consult AG is integrated into a national and international network. This enables us to provide comprehensive technological advice and support. We would be happy to provide you with references for the individual fields of activity:
- Consulting and scientific support of life science companies in the fields of preclinical, safety and regulatory affairs
- Toxicological reports according to § 24.2 AMG and REACh reports
- Expert opinion according to EMA/CHMP/ CVMP/ SWP/169430/2012: Shared Facilities
- Preparation of PDE reports according to EMA Guideline
- Toxicological reports on impurities in medicinal products and medical devices
- Valuation of extractables and leachables
- Preparation of Common Technical Documents (CTD, e-CTD)
- Support with approval-relevant questions/step-by-step plan procedures
- Feasibility studies for innovative products
- Manufacturing and control line according to § 15.1 and § 15.3 AMG
- Organisation and monitoring of clinical trials
- OEL/OEB assessments for pharmaceutical manufacturers
- Production of publications, press and public relations work
- Support and advice for VC/PE investments
- Preparation of PDE reports according to EMA Guideline
- Technology Due diligence
- Technology Turnaround
- Advice to investors (equity investments)