See you at the DIA Global Annual Meeting 2024!
Visit our Booth #2027

Schedule A Meeting
June 16-20, 2024 | San Diego, CA

See you at the DIA Global Annual Meeting 2024!
Visit our Booth #2027

Schedule A Meeting
June 16-20, 2024 | San Diego, CA

SCHEDULE A MEETING

    June 16-20, 2024 | San Diego, CA
    Maximize regulator confidence, Optimize safety compliance

    Enhance patient safety with our robust case processing, aggregate reporting, and signal management solutions. Increase regulator trust, and support market access through comprehensive, timely and accurate reporting while improving operational efficiency.

    Mitigate risks with REMS and Risk Management

    Unlock full market potential of your products by harnessing our expertise in developing Risk Management Plans (RMPs) and Risk Evaluation and Mitigation Strategies (REMS). Our strategic advice empowers you to navigate regulatory complexities across therapeutic modalities.Ā 

    Real-timeĀ Medical Information supportĀ to yourĀ Patients and HCPs

    Provide best-in-class support to your patients and HCPs with our 24×7 integrated response center offering support in 100+ languages through customizable, end-to-end Medical Information services.

    Improve drug development andĀ approval processes acrossĀ product life cycle

    Strengthen your drug approval process and post-marketing surveillance across your portfolio by partnering with our team of experts who take complete ownership of Regulatory compliance, generating high-quality clinical and regulatory documents throughout the product life cycle.

    Inspection Readiness with Unsurpassed Quality Assurance

    Elevate your processes with our expertise in setting up a inspection-ready Quality Management System (QMS). Our meticulously developed risk-based programs ensures compliance and provides you with peace of mind at all times.

    Your Trusted Partner

    Manage complexity and compliance with Best-in-class subject matter experts - delivery teams comprising 100% HCPs including 100+ physicians
    Comprehensive support across the development life-cycle, from proof-of-concept to post-approval management
    Reinforce global expansion plans with safety capabilities in 100+ countries and Medical Information coverage in 50+ countries across 100+ languages
    Expansive coverage of your portfolio through our diverse therapeutic area and product expertise
    puzzle
    Customized right fit solutions enabled through flexible delivery models
    Unparalleled quality, data privacy and information security with ISO 9001:2015, ISO 27701:2019, and ISO 27001:2022 certifications
    Technology-driven approach to comprehensive Compliance and Risk Minimization
    Brochures
    Case Studies

    Pharmacovigilance

    Medical Information

    Regulatory Affairs

    Medical Writing

    Latest from DIA Annual 2024

    booth1
    Marathon
    booth2
    Image

    How can we work together for better health?

      Please note that by submitting this form, you consent to your personal data being processed in alignment with our Privacy Policy. APCER is committed to ensuring the security and protection of your personal information. Your personal data will be processed for purpose of facilitating your request and may be used for sending you additional marketing and business development-related information about APCER Life Sciences, its affiliates and our services. You can withdraw your consent by writing to us at DPO@apcerls.com.

      Contact Us