Now a day’s, society demands the Regulatory Agencies to promote the entering of health products that will deliver benefits for the patients, whilst avoiding the entering of hazardous products to the market.
This growing pressure translates into requirements that have become more and more specific and restrictive; and coping properly with such requirements, depends heavily on the expertise of the CRO in the regions and countries of interest.
Use the expertise of Latin American CRO MMATISS to reduce the time invested to achieve regulatory approval, one of the most important milestones in any product development program.
The expertise of Latin American CRO MMATISS is put to your service, to support you with:
- Submissions for Protocol/ Investigational Site approval,
- Submissions for Importation/exportation approval,
- Safety Report submissions
- Submissions for marketing authorization.