Omni-EDS is an early development solutions provider. We work with early development projects and help shepherd them from preclinical through proof of approval. Our focus is on ensuring the development of a life sciences product is done with the end commercial goal in mind. All our subject matter experts are proven specialists in drug development, regulatory and medical writing, each with over 20 years of background experience. They assist clients with anything from defining the best development-commercialization pathway for your product to finalizing a regulatory submission. 

Delivering authentic healthcare innovation is more challenging today than ever before! The overall probability of drug development failure is estimated to be more than 88%. Many compounds do not make it because it takes experienced personnel who have regulatory compliance knowledge and understanding, strong manufacturing acumen, and complex project management capabilities to progress a product candidate.

Successful drug development demands a sharp focus on the customer need. It requires the development and delivery of data, knowledge and products that make a difference.  Omni-EDS experts bring years of successful drug development experience to your team and the knowledge to avoid common pitfalls. Learn More

Both major multinational pharmaceutical corporations and small, innovative biotechnology companies need access to quality Regulatory Affairs to optimize the market application. Omni-EDS experts have the breadth of knowledge to help with a wide range of regulatory needs. Learn More

Whether you are looking for technical, clinical or regulatory writing, Omni-EDS medical writers can help develop, organize and publish submissions, ​grants and manuscripts. Learn More