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Stark Pharma Showcases Global Expertise at BioAsia 2020 – Booth #45

Stark Pharma was proud to participate in BioAsia 2020, held in Hyderabad, India from February 17th to 19th, representing our commitment to advancing life sciences through a unique blend of regulatory expertise, clinical support, and IT-driven solutions.

At Booth #45, we welcomed hundreds of visitors from pharma, biotech, medtech, and digital health sectors, introducing them to our robust service portfolio across CRO Services, Regulatory Affairs, Pharmacovigilance, Medical Devices, and IT Services.

Featured Services:

CRO Services

    • Clinical Operations
    • Regulatory Affairs
    • Pharmacovigilance
    • Validation
    • Biostatistics & API/RLD Sourcing
Medical Devices
    • Labeling
    • US FDA Submissions (510(k), PMA)
    • EU MDR Compliance
    • Post-Market Surveillance (CAPA, PMS, PRRC)
Drugs & Biologics
    • CMC
    • Medical Writing
    • Labeling
    • eCTD Publishing
    • Regulatory Audits

IT Solutions by Stark Pharma:

  • Stark QMS – A purpose-built Quality Management System (QMS)
  • Custom Applications – Regulatory, clinical, and quality solutions tailored for life sciences
  • Complaint & CAPA Systems – For global post-market compliance
  • End-to-End Support – Including product development, implementation, and long-term maintenance
For meetings, please contact sales@starkpharma.com