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Services from Clinical to Commercial

Manufacturing parenteral products presents numerous high-stakes challenges: formulation and reformulation issues, delivery system conversion, upscaling from clinical to commercial production, market fluctuations in demand, new indications, emerging markets, risk mitigation, patent expiry and more. As your development and manufacturing partner, we are committed to collaborating with you to overcome such challenges, utilizing our clinical-to-commercial range of services — customized to your explicit needs — with the goal of maximizing product quality and speed to market.

Explore Our Services

  • Formulation Development

    Leveraging our scientific and technical expertise in sterile-injectable manufacturing partnerships.

  • Lyophilization Cycle Development and Optimization

    Using advanced technology to assist clients with lyophilization cycle development and optimization.

  • Rapid Technology Transfer

    Ensuring rapid technology transfer through strong partnership.

  • Fill/Finish Operations

    Precisely coordinating our fill/finish operations to ensure quality and timely delivery of product.

  • Specialized Containment

    Utilizing restricted access barrier system technologies to ensure safety and regulatory compliance.

  • Analytical Services

    Offering robust analytical capabilities to ensure stringent quality assurance and precise testing.

  • Global Regulatory Support

    Providing expert guidance to help clients execute regulatory strategies and prepare filings.

Contact Us

Learn more about how our services can help you optimize your product’s potential.