Regulatory as a Service: Addressing Compliance Challenges

About the webinar

Watch our webinar to learn more about integrated, end-to-end Regulatory as a Service (RaaS) offering that leverages leading technical solutions, including Amplexor Life Sciences Suite and RIMExpert:

In 60 minutes you’ll learn:

• The benefits of an integrated end-to-end RaaS bundled solution
• How an integrated, RaaS offering aligns with a holistic regulation information management (RIM) platform
• How to deploy a more efficient and cost-effective platform to ensure regulatory compliance

About the speakers

Rajiv brings more than 15 years of experience in Pharmaceutical R&D, Regulatory, and Digital sectors. He has comprehensive strategy and operations experience in advising top global Pharmaceutical companies, especially in leading large scale transformation programs, including mergers and acquisitions, Brexit, and Digital Transformation.

At Genpact, Rajiv leads the Regulatory Affairs practice globally and is responsible for driving profitable growth for the business. In addition, his role entails enhancing the go-to-market approach, actively pursuing strategic partnerships and acquisitions, building innovative offerings, and supporting critical client engagements.

Prior to Genpact, Rajiv spent more than ten years in the Management Consulting industry working for The Boston Consulting Group and Capgemini Consulting where he led multiple Corporate, R&D and Regulatory Affairs programs for Pharma companies.

With more than 30 years in the Pharmaceutical industry, Kevin has worked in Regulatory CMC at Wyeth and Pfizer – and other top ten healthcare companies. He has broad experience from his leadership roles in Quality, Manufacturing, Supply Chain, Technical, Regulatory, and Compliance.

In previous roles, Kevin managed critical regulatory Compliance initiatives and implemented global processes through the product lifecycle. He established and implemented global regulatory organizations, regionally based, focused on meeting the requirements of the regulatory authorities and improving the efficiency and compliance of new submissions and variations.

His extensive experience working with international regulatory Health Authorities and emerging markets has further positioned him to manage global submissions and simultaneous product launches in multiple countries.

With more than 25 years of experience in the Life Sciences industry, David is a seasoned executive with extensive experience delivering solutions to clients, with a particular focus in the areas of content management and collaboration.

In his current role in the Life Sciences division of Amplexor, David’s primary focus is aligning customer needs with the capabilities of the company’s Life Sciences suite to ensure that the solution meets the needs of the customer.

David also leads the DIA EDM Submission Reference Model team, which has developed a document architecture for use when designing and building content management solutions. This architecture has been leveraged by numerous companies and vendors to provide submission management solutions that are compliant with global regulations.