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 ServicesRegulatory AffairsPharmacovigilanceMedical 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