The corporate mandate of SPharm is to offer high quality and personalized Pharmaceutical/Medical Regulatory Affairs, Product Development and related services, always performed with professionalism and integrity.

Offering much more than just regulatory consultation or dossier preparation, SPharm provides the advantages of a true partnership by ensuring that its services are fully integrated with your company’s processes, procedures and strategic objectives.

Our services will suit your various regulatory and product development needs:

• Product development expertise and guidance to help navigate the complexity of the regulatory world;
• Establishment and strengthening of regulatory liaison and constructive dialogue with Health Authorities;
• Obtain authorization for the conduct of clinical trials in Canada;
• Preparation of various quality regulatory dossiers in a timely manner;
• Ensuring the compliance of your key regulatory documents such as product monograph and chemistry/manufacturing summaries for your approved products;
• Establishment and maintenance of a quality system to ensure compliance with Good Manufacturing Practices in preparation or following market authorization for importation/distribution in Canada;
• Establishment of a working partnership that is reliable and efficient to help streamline the regulatory workload when needed, and consequently assisting our client in meeting their corporate objectives.

Please see our Services section for more details.

To find out more about the quality and scope of services we offer, in both English and French, please contact today Susanne Picard, President, Tel.: (819) 824-6869.