ABOUT

Cerenos Group is a deeply experienced group of consultants with a proven track record in bringing products to market efficiently.

Integrated Approach

Cerneos Group is a seamless, consolidated team dedicated to serving all international medical markets to efficiently bring innovative life sciences products from concept to commercialization.  

Our integrated approach has been successfully used by large and small firms to launch products in the US and overseas.

Meet the Cerneos Group

  • Richard C. Tharin, MS, RAC
CEO/Founder Chief Regulatory Consultant Red Cross Tissue Services, NIAID/NIH, Terumo Medical, Kimberly Clark, US Navy

    Richard C. Tharin, MS, RAC

    CEO/Founder
    Chief Regulatory Consultant

    Red Cross Tissue Services, NIAID/NIH, Terumo Medical, Kimberly Clark, US Navy

    BIO
  • Joseph Kavanagh BSc, MBA, Senior Consultant | Business and Development Strategy | Market Analytics | Medicare and Payer Reimbursement; Pfizer, Merck, Novartiz, Grifols

    Joseph Kavanagh BSc, MBA

    Senior Consultant | Business and Development Strategy | Market Analytics | Medicare and Payer Reimbursement

    Pfizer, Merck, Novartiz, Grifols

    Bio
  • Richard Reeves, BASc, MBA
Senior Regulatory Affairs and Quality Assurance Consultant
RAPS, Varian Medical Schools, Intuitive Surgical

    Richard Reeves, BASc, MBA

    Senior Regulatory Affairs and Quality Assurance Consultant

    RAPS, Varian Medical Schools, Intuitive Surgical

    Bio
  • Tom Catalano, PhD
Senior Regulatory Affairs Consultant

    Tom Catalano, PhD

    Senior Regulatory Affairs Consultant

    Bio

Our Services

We develop basic assets and technologies into commercially viable products through our science, finance and strategic partnering alliances. 

  • We provide global regulatory strategy, submission development, and clinical trial coordination for biotech, device, diagnostic, and pharma products, working with international health authorities such as FDA, Health Canada, MHRA, ANVISA, PMDA, CFDA, and KFDA.

  • We conduct scientific research feasibility studies, develop pre-clinical safety evaluations, and provide technical and CMC documentation for design, patent, and regulatory submissions. Our services also include grant proposal writing for agencies like NIH, NSF, DoD, BARDA, DARPA, and NASA, as well as human factors and usability evaluations for medical devices, diagnostics, and software.

  • We provide team development, project management, and resource acquisition, along with financing and fundraising support for startups and established firms. Our services include strategic partnerships, global supply chain support, U.S. agency coordination for international life science and med-tech firms, and soft landing services for innovators in multiple regions.

Global Regulatory Agency Experience

US, Canada, Australia, UK, EU, APAC, Brazil, LATAM

RAPS Code of Ethics

Cerneos Group is an active member in good standing with RAPS (Regulatory Affairs Professionals Society) and proudly abides by the RAPS Code of Ethics.