About Business

Business Summary

Regulatory Affairs Consulting Firm- Best regulatory affairs consulting firm in the Middle East and Africa region.

Business Description

MERAS Consulting - To contribute in the ultimate purpose of improving patients’ lives, MERAS’ vision is to facilitate journey for the biopharmaceutical and medical device industries aiming to commercialize their therapies in the MEA region.

Pharmaceuticals, Biological products, Biotechnology, OTC, Medical Devices, Cosmetics, Food supplements, Vitamins, Herbals, Nutritional products, Veterinary products, Orphan drugs

Regulatory Affairs Consulting Firm. Best regulatory affairs consulting firm in the Middle East and Africa region. With offices based in Egypt and UAE, Regulatory Consulting.

Regulatory affairs consulting firm, Regulatory affairs services, Regulatory affairs middle east, Medical device registration, Pharma registration middle east, Regulatory intelligence, Regulatory strategy, Regulatory submission , Regulatory authorization, Regulatory Reviewing, Pharma Labeling and Artwork, Regulatory Databases and archiving systems, Market access, Distributor Management, Regulatory Training, Regulatory Affairs outsourcing, Regulatory Partnering.

Providing solutions that exceed our customer expectations and needs, complying with the local and global laws and regulations.

In 2009, MERAS Consulting set up with the goal of serving the Middle East and Africa as its overall target. Because our operations are based in Egypt and the United Arab Emirates, we have had a powerful and strategic presence throughout the region because of our regional experts and experts working in both places. In a very dynamic market, MERAS experts can perform a broad range of analyses, as well as integrating a regulatory compliance program. From merely consulting on a particular issue to serving as our company's regulatory and Pharmacovigilance partner.

Products / Services

Services

• Regulatory Intelligence
• Regulatory Strategy
• Product Registration
  Regulatory Documents Review
• Labeling and Artwork
• Documentation and Archiving
• Market Access
• Distributor Management
• Regulatory Affairs Training
• Regulatory support
• Pharmcovigilance regulatory