Regulatory Support

Algorithme Pharma's experienced regulatory team consistently produces high quality submissions, ensuring key clinical trial milestones are met on time.

Regulatory support services include :

  • Coordination of IRB submission
  • Preparation of pre-CTA and pre-IND package
  • Coordination with the regulatory agency for pre-CTA/IND meetings
  • CTA preparation
  • Submission to Health Canada
  • Negotiation and clarifax responses

Regulatory Affairs

Our Scientific & Regulatory Affairs Department is involved in regulatory discussions to assure that the goal of your study meets the requirements of corresponding authorities.

Medical Writing

We have developed a strong reputation for delivering a high quality, reliable and responsive medical writing service. Our dedicated team of professional medical writers provides a complete writing service to clients around the globe...

Scientific Affairs

Once your needs have been clearly identified, the Scientific & Regulatory Affairs Department will prepare a study design that best accommodates development needs and effective study conduct.

Quality Assurance

We are committed to the provision of accurate, rapid and reliable results.

Bioanalytical Services

The Bioanalytical Services Department offers scientific excellence, uncompromised quality and unbeatable timelines to meet and exceed client needs.

Clinic

We have 25 years of experience conducting clinical trials. Our Montreal, Québec, clinic has 265 beds, while our Fargo, North Dakota, clinic (under the leadership of Dr. James Carlson) has access to 200. The beds are located in fully equipped clinical units, including a dedicated long-stay unit.