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IN2Pharma offers a broad range of consultancy services to the Pharmaceutical and Healthcare industry. Our team provides expertise and services in Regulatory Affairs, Medical Affairs and Quality Assurance.

Quality Assurance
IN2Pharma has an extensive experience in Quality Assurance. We support companies in the set-up and maintenance of a GMP and/or GDP compliant Quality Management System by writing SOPs, implementing CAPA plans, preparing technical agreements, executing audits, providing support during pharmaceutical inspections, etc. Our Qualified Persons will guide you in a pragmatic way to GxP compliance!

Medical Affairs
IN2Pharma offers a full range of Medical Affairs services, from the development of scientific trainings and expert reports up to the set-up and maintenance of Pharmacovigilance systems. We also provide pharmacovigilance training to sales reps, advertising rules to product managers, etc. Our Qualified Persons responsible for Information & Publicity advise on compliance of promotional material as well as interactions with healthcare professionals and organizations, both in Human Pharma and Animal Health. Struggling with the transparency reporting of transfers of value? We are your one-stop-shop solution!

Regulatory Affairs
IN2Pharma provides a broad range of Regulatory Services from initial strategic advice and product development to preparation, submission and maintenance of Marketing Authorisations for (herbal) Medicinal Products. But also the preparation and maintenance of Technical Files for Medical Devices and notification dossiers for Cosmetics and Nutrients falls within our expertise. We offer Regulatory Intelligence for medicinal and healthcare products in Benelux!