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Dossier submission, preparation or review and filing

Development of regulatory strategy for the product’s life cycle

Facilitate interaction with regulatory agencies, such as in meetings and conference calls, negotiations during development stages, submissions and submission approval process

Regulatory classification of products across different jurisdictions

Pharmaceutical Product Development Services include Compliance activities, including development of compliance programs and conduct of facility audits for adherence to GLP and GMP standards

DRA Solution, Inc.

Pharmaceutical and Healthcare Consulting Services

We are regulatory affairs consultants assisting companies to plan and manage their pharmaceutical and medical product development programs and regulatory requirements for the Middle East Region. Our qualified experts can provide advice from the early stage of pharmaceutical development to the marketing applications.

Our Services