Bioequivalence

Algorithme Pharma's Industry leading report timelines and expertise with a vast number of compounds, have led to our excellent reputation for complex Bioequivalence / Bioavailability trials and submissions. Our full service offering supports all aspects of generic drug development. Full-time physicians oversee all aspects of a trial and we continuously monitor our regulatory compliance against international regulatory guidance as well as numerous operational metrics including on-time Recruiting and Reporting.

Recruitment

Recruiting is crucial to the clinical trials process. Our effective approach to recruitment is two-fold.

Clinic

Algorithme Pharma has over 20 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.

Data Management

Algorithme Pharma has extensive data management expertise. The quality and integrity of clinical data being entered into our database is a key priority for us.

Project Management

High quality project management is key to the success of a clinical trial.

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.

Bioanalytical Services

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

Quality Assurance

Algorithme Pharma is committed to the provision of accurate, rapid and reliable results.

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...

Pharmacokinetics and Pharmacodynamics

The Algorithme Pharma team provides extensive pharmacokinetic (PK) and pharmacodynamic (PD) support in preclinical and clinical studies.

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.

Statistical Services

Our team has extensive experience in providing a wide range of statistical services.

Clinical Sample Kits & Management Support

Preparing, collecting and shipping clinical samples from trial sites to bioanalysis laboratories is a critical support service when managing clinical programs.