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Quality and Compliance

We support pharmaceutical and biotech companies in the reliable, secure delivery of life-saving and life-sustaining drugs to their patients.

Quality is our highest priority

As industry leaders, it is built into everything we do and is an area of continuous focus and investment. For our clients, we provide solution-driven, appropriately engineered and skillfully tailored regulatory approaches. Our experts think creatively and work within regulatory guidelines, to deliver practical, compliant solutions.Our team has deep expertise and broad experience in dealing with global regulatory authorities and consulting clients, from large pharma to virtual start-ups.

Quality Management System (QMS)

Our full suite QMS, QualityOne, helps ensure we operate to a consistently high and harmonized standard to meet the needs of a global market. Implemented across our global network of GMP facilities, QualityOne unifies our approach, strengthens compliance and decision-making and enables us to provide enhanced document management, electronic change control capability, corrective and preventive action (CAPA) and deviation management.

Quality Culture

Every member of our team is committed to delivering impeccable standards and results.We have developed programs to certify staff in quality principles and created numerous dedicated roles within our organization. Ongoing training is in place for all our associates. Specific to their job and functional areas, our training programs ensure associates are well versed in all aspects of quality, its importance and how all our people contribute to quality assurance.

Robust processes

All starting materials are checked by trained quality control personnel at incoming against specifications to ensure quality and any deficient lots are quarantined.
Testing on packaged products is performed by certified teams and the results are documented in the batch record and reviewed by our quality department prior to release.

We have a deep commitment to quality, exceptional credentials and a history of strong regulatory compliance.

Accreditations

Our quality credentials

    • US Food and Drug Administration (FDA) registered and inspected
    • US Drug Enforcement Agency (DEA) registered and inspected
      European Medicines Agency (EMA) approved
    • Brazilian National Health Surveillance Agency (ANVISA) approved
    • UK Medicines and Healthcare Products Regulatory Agency (MHRA) approved
    • Russian The State Institute of Drugs and Good Practices (FSI SID&GP) approved
    • Turkish Medicine and Medical Devices Authority (TİTCK) approved
    • Australian Therapeutic Goods Administration (TGA) approved

Local work, global impact

  • Leadership

    The Sharp leadership team is comprised of industry experts who offer broad experience and real vision. Their knowledge of the bio/pharma, clinical trials and packaging industries give Sharp a deep understanding of the challenges our clients face.

    Leadership
  • Sustainability & ESG

    We are committed to limiting the impact we have on the environment and helping to protect our planet for the generations to come.

    Explore our commitments to sustainability
  • Our Facilities

    Sharp’s network of GMP facilities across the US, UK and EU offer global reach, production scalability and risk mitigation through the validation of multiple identical lines across our network.

    View all our facilities
  • About Sharp

    Sharp is a leader in commercial packaging, clinical services & sterile manufacturing with a heritage spanning more than 70 years.

    Learn more about us
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