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Rashmi P

Rashmi P

Healthcare Compliance Consultant

Overview of Experience

Healthcare Compliance and Ethics professional with over 12 years of experience in the Pharmaceutical/Biotech Industry. Proficient in delivering smart, automated, and integrated compliance solutions. I have set up and managed compliance teams to ensure interactions with HCPs, HCOs are compliant, all activities with external stakeholders including Third-parties are conducted in-line with the anti-bribery policies, and materials are in compliance with Industry Codes at the EU and UK level.

Areas of Expertise

Building compliance programs.

Setting up compliance monitoring systems and processes on SharePoint.

Rolling out compliance training.

Drafting and rolling out SOPs.

Running Compliance Committees.

Lead the set-up of the Transparency program and its implementation.

Fair market value assessments.

Setting up end-to-end engage to pay processes.

Maturity Assessment.

Incident Management/ CAPA.

Track Record

This includes:

  • Gap Analysis, Building Policies, Principle documents, Guidance and SOPs.
  • Providing Compliance guidance and support for set-up of Promotional compliance systems and processes e.g. Veeva PromoMats, Veeva Events Module, Veeva CRM, Set-up of processes like FMV, Risk Assessment and management and providing compliance-related guidance/advice to enable the business to take a risk-based decision.
  • Project Management experience (Prince 2 qualified) to support the set-up and management of the compliance infrastructure and provide strategic business support.
  • Strong influencing skills, ability to manage complex situations tactfully and always have a solution-oriented approach.
  • Experience of working with the local and international markets, work very closely with the legal department, Market Access, Medical Affairs, Commercial, Finance, Procurement, Digital and R&D departments.
  • Expertise with complete set-up and management of SharePoint and Intranet sites for the Legal and Compliance team and also with Data Analytics tools like Power BI and Tableau.
  • Staying up to date with changes to the legal framework and regulations impacting the pharmaceutical industry in the EU.