With experience across all four routes, Taw Pharma® provides regulatory support and guidance throughout the application’s lifespan. We can compile and submit dossiers in eCTD format and support you getting your product to market as efficiently as possible. We then work hard to ensure it stays there.
We can create full eCTDs for new applications as well as convert dossiers in part or whole for older MA applications and variations. We also have extensive experience in Post Marketing Maintenance, maintaining your product by conducting licence transfers, variations, renewal applications, reclassification of medicines and Periodic Safety Update Reports (PSURs) to ensure that your product continues to meet the necessary standards of safety, efficacy and quality.
Taw Pharma® can act as applicant for your procedure in the UK or Europe as we have offices in both the UK and the EU.
Taw Pharma® is part of the Jenson group of companies. The specialist team at Jenson R+ Ltd is experienced in regulatory affairs, product development, quality assurance, drug safety, medical information, copy approval, project management, training and market access. JensonR+ can provide support at all levels, from strategy through to administration, which allows us to tailor our services to meet your specific needs as your company moves from innovation and development to the market place.