Manufacturing & Quality
Vidalife Pharma specializes in Pharmaceutical Finished Dosage Formulations / APIs for the Regulated/ Semi Regulated markets.
We ensure our clients are satisfied with our high quality of products at affordable prices.
We also provide third party audits or pre-audits for our clients to ensure the facilities are up to the international standards.
Vidalife Pharma also has tie ups with numerous manufacturing facilities. These State-of-the-Art CMOs are EU/US approved and follow the cGMP standards of production.
REGULATORY SERVICES
At Vidalife Pharma, we understand Pharmaceutical Technicalities involved in Product Development and Filing of the dossiers.
The Onus lies on the Strong & Well experienced Team to understand the scope of development and leverage unmatched Productivity, Efficacy & Quality.
Our management consulting services focus on our clients' most critical issues and opportunities:
· Product Development
· Documentation
· Dossier Development
· Regulatory Affairs
· Formulation Development
· Manufacturing Process Development