Pharmaceutical

American CIT’s Pharmaceutical practice provides clients with full-service Medical Affairs offerings, bringing innovation, integration and experience to drug development, clinical trials and the approval process.

American CIT staff includes medical doctors with both clinical and industry experience in various therapeutic areas. Their support ensures persuasiveness and high level of credibility through proper interpretation of the data generated, correct positioning of the products in relation to current therapeutic options and rewarding contacts with opinion leaders

Regulatory Affairs

The American CIT regulatory group knows the process involved in obtaining a product registration. Our skilled team works with you to prepare and complete global or local submissions, and interacts with regulatory agencies to enhance successful authorization.

American CIT delivers the insight and expertise of clinicians, regulators, scientists, and health economics experts with competencies that cover every aspect of the drug development process. Our services are available across multiple therapeutic specialties

Post Marketing Surveillance (PMS) Programs

Marketing

Quality Assurance

Medical Writing