Impact Pharmaceutical Services Competitors

MVG Consulting Services specializes in helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs. We can provide start-up and virtual companies with the necessary resources to begin their clinical development program. We also help well-established companies with staffing needs on an as needed basis for both short and long term projects. Established in 1998, MVG Consulting provides companies an alternative to large CROs. Services provided by MVG include but are not limited to: Clinical Quality Assurance Clinical Operations Project Management Medical Writing MVG provides highly qualified clinical research professionals who seamlessly become a part of your project team. Additionally, we can provide virtual companies with an entire project team that encompasses all aspects of clinical development. Contact us to learn more about MVG Consulting and how our team can help you meet your clinical drug development objectives.

Velesco applies nimblocity to your early stage drug development projects, with our proven formulation of expertise, flexibility, dedication, and velocity to clinic. Expertise and experience Velesco is a CMC contract research organization, founded and staffed by pharmaceutical scientists from Pfizer's former Michigan R&D campus. Our team has experience with more than 100 drug development programs. Flexibility Our nimble processes and focused expertise enables us to overcome even the most challenging obstacles. Our team is responsive, accommodating, and eager to help you reach the full potential of your compound, quickly and efficiently. Personalized Partnerships We treat your project like it's our own and share everything from insightful observations to solutions for problematic analytic methods, to assistance with the FDA registration process. All our services are royalty-free. Velocity to clinic We're committed to getting your compound to the clinic on time. Our size, capacity, and expertise allow us to accommodate changes swiftly while maintaining control and quality. As experts in pharmaceutical analytical chemistry, drug formulation development, and cGMP clinical supply manufacture, Velesco scientists have a proven track record of moving compounds through the critical drug development process with nimblocity and unrivaled success.

Established in 2001, Drug Discovery Alliances, Inc., is a minority-owned, US-based pharmaceutical research and development consultation firm specializing in establishing alliances to facilitate pharmaceutical R&D. Drug Discovery Alliances provides a small molecule and biologics R&D platform backed by a team of CMC consultants and a global portfolio of vetted suppliers. By leveraging the DDA platform enables our clients to overcome many challenges one faces in driving small molecule and biologic programs from discovery to commercialization. Areas of focus including developing robust syntheses to lower cost of API’s, backup supplier mitigation, and incorporating technology based solutions to overcome manufacturing challenges are just some of examples of how we have helped our clients. Our alliance partners provide the following services spanning the R&D continuum including: medicinal chemistry, in vivo studies, in vitro studies, process research, cGMP API manufacturing, RSM manufacturing, commercial manufacturing, formulation, crystallization R&D, drug product manufacturing, sourcing, generic API sourcing, GMP audits, CMC consulting, regulatory consulting, and assisting companies with licensing and fund raising activities.