Quality & Regulatory Adviser

Dr Nishita Trivedi

Dr Nishita supports the planned quality and regulatory framework, including QMS, GDP, PLPI activities, vendor oversight and MHRA liaison.

Specialist adviser described in the business plan; not a statutory director
Executive profile

Responsibilities grounded in NovaPharm's operating plan.

NovaPharm's business-plan materials describe Dr Nishita as an experienced pharmaceutical quality and regulatory professional with approximately 20 years of experience across quality systems, GMP and GDP compliance, audits, validation, data integrity, CAPA, pharmacovigilance support and regulatory liaison.

Her experience includes responsible-person duties within UK pharmaceutical organisations. Any formal Responsible Person or RP(i) appointment for NovaPharm would remain subject to the applicable authorisation, governance and regulatory requirements.

Dr Nishita is not presented as a director or shareholder of NovaPharm Healthcare. Private contact information and CV-specific personal data are not published.

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