Menu
...

Regulatory @ Transintegra

________________________________________________________________________________________________________________________________________________________________________________________

Speed up the Regulatory Decisions

You may need to urgently compile regulatory dossiers for submissions in new markets or for license renewal in existing markets

Or, there could be old products, which do not have ICH-CTD or a CTD of specified regional format & you wish to get it done at low cost, quickly

Or there could be critical Health Authority commitments leading to update of regulatory documents

On such business needs, why wait, when the business goals can still be achieved with the same consistency, speed, accuracy, at a lower cost, without hiring/training additional staff on such short-term business priorities.

555;58;d50ea85c657e3a5863c9346e54cc61abe1791c0f555;58;4ef900ad1ec779b617aa5447793ebdcdd188027e555;58;69b60db65aec43388362b5a60b1493a4c579b56a555;58;9ccb175700fe5565b0e0709b991ac35797bc2bf9

Our regulatory input is backed by years of industry experience. We have successful experience in managing Regulatory Affairs activities for South Asia, ASEAN, Latin America, Korea, Australia-NZ and Africa. From Regulatory Strategies to compilation of different regional dossiers, product registrations & managing Health Authorities Queries. Transintegra can provide Regulatory Support to full-fill the business needs.