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December 2, 2020

Together for efficient support

Medical Affairs

APCER Life Sciences provides the medical resources you need to listen to the market, respond to opportunities, and communicate with timeliness and accuracy.
Scientific communication is growing not only in complexity and specialization, but also in the number of publications, channels, and audience types. With experience across all major therapeutic areas, APCER helps life science companies meet the increased demand on Medical Affairs.

Monitor and analyze KOL opinion and competitive claims
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Develop the right studies to demonstrate value compared to alternatives
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Communicate to a business-oriented, cost-constrained audience

Scientific Content

APCER has the medical knowledge and writing disciplines needed to create scientific content for continuing medical education programs and advisory boards.

Patient Support Programs

APCER provides inbound and outbound communication to improve patients’ understanding of the disease, their compliance with medication, and ultimately their care and relief.

Investigator-Initiated Studies

APCER customizes solutions to support clinical studies being undertaken by independent physicians or research groups to gain regulatory approval for additional indications.

Multi-Channel MSL Solutions

APCER builds teams of Medical Science Liaisons (MSLs), who maintain close rapport with physicians and help propagate understanding of the disease and the science behind the product, through traditional and virtual communication methods.

Reimbursement Dossiers

APCER supports the creation of reimbursement dossiers in its varying formats across major markets to highlight the value proposition and cost effectiveness of a new drug versus existing treatments.

Health Technology Assessments

APCER’s resources integrate with yours to evaluate the social, economic, organizational and ethical issues of a health intervention and inform policy decision-making.

Together, a trusted voice

Activities to educate and communicate with external stakeholders are moving out of Commercial departments and into those with medical and clinical expertise, just as the supply of medically trained personnel and the budget to pay for them are decreasing. APCER provides highly qualified and affordable resources, who work together with your team, to become the most trusted voice for your products.

The APCER Advantage

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Domain Expertise
  • 100+ physicians, 90% healthcare professionals supporting drug safety and Pharmacovigilance
  • Experience and expertise in different product types including Drugs, Vaccines, Biologics, Biosimilars, Cell and Gene Therapy products / Advanced Therapy Medicinal Products, Medical Devices, and Combination products
  • Medical and scientific writing to support global product approval and post marketing requirements
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Client Focus
  • Scalable and flexible operating models
  • Strong governance with collaborative approach
  • Outcome-driven engagements
  • End-to-end Pharmacovigilance, Medical Information, Regulatory Affairs, Quality Assurance and Medical Writing activities throughout the Product lifecycle
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Global Presence
  • Presence in US, UK, Europe, and Asia
  • Safety reporting capabilities in 100+ countries
  • Medical Information coverage in 50+ countries and 30+ languages, scalable to 100+ languages
  • Developing and contributing to regulatory strategies, to maintain global regulatory compliance across the product life cycle
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Quality and Compliance
  • Extensive experience in supporting successful Regulatory Inspections
  • ISO accreditations received:
    ISO 9001:2015 (QMS)
    ISO 27001:2013 (ISMS)
    ISO 27701:2019 (PIMS)

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Testimonials

  • Medical Advisor, Medical Affairs
    I must commend the organizational skill, the professionalism, the clarity, the expertise on subject matter, execution excellence that APCER has exhibited in all my projects where I had collaborated…
    Medical Advisor, Medical Affairs
    A leading bio-pharma company
  • Global Clinical Leader
    My experience with APCER has been excellent. The team was very helpful, knowledgeable, responsive and professional with all the work that was needed.
    Global Clinical Leader
    A leading pharmaceutical company
  • Associate Submission Medical Writer
    APCER demonstrated extreme flexibility accommodating changes, and a number of last-minute changes were implemented quickly and correctly. I also appreciate the flexible communication during my workday, given the time zone differences between the APCER writers and myself.
    Associate Submission Medical Writer
    A leading bio-pharma company
  • Medical Director
    APCER’s speed, responsiveness and flexibility to meet our safety needs is something we have always valued. APCER has helped harmonize our global pharmacovigilance operations and made us compliant with ever changing regulations.
    Medical Director
    US-based specialty pharmaceutical company
  • QPPV and Pharmacovigilance Head
    The audit was carried out professionally and objectively. The scope of the audit was relevant and appropriate, and time efficient. The discussions during the audit were constructive and recommendations where helpful and appropriate. The team members involved in the audit had a positive experience and were made to feel at ease by the auditors.
    QPPV and Pharmacovigilance Head
  • Senior Director
    We are thankful to team APCER for bringing in strong practices & helping inspection readiness in our pharmacovigilance framework which led to successful FDA audits.
    Senior Director
    US-based pharmaceutical company
  • Head, Clinical Trial Transparency
    APCER’s invaluable support with Clinical trial disclosure deadlines helped us in timely submissions of periodic reports.
    Head, Clinical Trial Transparency
    Top 10 pharmaceutical company with operations in the EU and US
  • AVP, Pharmacovigilance
    We appreciate APCER for its efficiency in responding to matters that they get even at the eleventh hour. Working with APCER has made compliance a lot easier.
    AVP, Pharmacovigilance
    US-based pharmaceutical company
  • Senior Director
    We are thankful to team APCER for bringing in strong practices & helping inspection readiness in our pharmacovigilance framework which led to successful FDA audits.
    Senior Director
    US-based pharmaceutical company

How can we work together for better health?

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    APCER Life Sciences is committed to improving health in partnership with its clients. We bring together safety, medical, regulatory and technology resources to ensure that patients receive the safest, most effective therapies possible.

    We are an ISO 9001:2015, ISO 27701:2019 and ISO 27001:2022 certified company.

    ©2025 APCER Life Sciences, Inc. All rights reserved. | Privacy Policy | Web User Agreement

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