The purpose of a feasibility study is to determine the applicability of a project against factors such as cost, time, resources, investigator interest, local medical practices and study competition. ...

Over the years CONVEX has created and now maintains and continuously expands its own database of Investigators all over the country, each one being a prominent figure in their field of expertise and ...

CONVEX prepares a preliminary and, upon further information by the Sponsor, a detailed Study budget of a clinical trial to be conducted, taking into consideration the lowest possible costs. The ...

On behalf of clinical trial Sponsors, Convex negotiates and enters into Agreements directly with investigators, medical institutions, local laboratories, courrier companies, disposal of materials ...

Now that Bulgarian legislation regarding clinical trials is fully harmonized wih EU legislation and guidelines, CONVEX’s large experience in regulatory submission is an even more invaluable ...

Convex performs on-site monitoring to ensure protocol and regulatory compliance and timely submission of data. Our monitoring team consists of full-time Clinical Research Associates (CRAs) who ...

Our experience and strong relations with local laboratories ensure the best choice of certified laboratory services, in accordance with the clinical trial design and at the most beneficial prices and ...

The success of a clinical trial heavily relies on the effective interaction of all professionals involved in the project. CONVEX uses agile project management design and planning to ensure safety, ...

Essential documents, such as clinical protocol, project plan and data management plan set the standards and requirements of a clinical trial. A quality control system should be at the center of any ...

Patient safety is a priority at CONVEX. It is what forms the basis of our uncompromised expedition and accuracy in reporting serious adverse event. Our MDs are experts in safety evaluation and ...

Medical Writing Services we offer:   • Protocol development • Investigator's Brochures • Case Report Forms • Patient Diary • Informed Consent Forms • ...

Sound knowledge in regulatory affairs does not merely provide benefits to a pharmaceutical, biotech or medical devices company. It is essential for its success. The more the industry grows globally, ...