Pharmaceutical Consulting Services
Turio Ltd. was established in 2004 and is an international pharma consulting services company for the pharmaceutical industry based in London and Oxford, UK. Turio Ltd. offers a comprehensive range of drug development, technical, regulatory and management services to pharma, biotech and private investing companies.
Advice and support is provided by a team of core independent pharmaceutical consultants, recognized experts in their field. These consultants collectively have several decades of drug development, regulatory and GMP compliance experience in the pharma, biotech and National Agencies within European Union and US FDA. The highly qualified team is assisted by a network of professionals who cover all areas of pharmaceutical and biotechnology expertise.
Our consultants have been particularly successful in assisting clients in Central Eastern European and Asian Countries, the European Union - EU, as well as the United States - US.
Examples of completed pharma consulting services projects:
- Pre-clinical development to IND submission of a lead candidate in oncology
- Complex pharmaceutical products (long release parenterals) and biosimilars development on behalf of a large generic company
- Due diligence of in-licensing opportunities on behalf of big pharma and generic companies
- M&A due diligence audits - technical, regulatory, GMP, compliance
- GMP compliance audits, mock PAI (pre-approval inspections) and advice in responding to FDA 483 observations and EU inspection deficiencies provided by ex-FDA and MHRA inspectors
- Regulatory strategy and support from early phases of drug discovery and drug development to approval for marketing, scientific advice and assistance with pre-submission meetings with EMEA and FDA
- Project management of complex products development and regulatory submissions
- Varied pharma consulting services for clients in Central Eastern European and Asian Countries, as well as European Union