Logo
Logo
bg-grid

Streamline Your Compliance with PMCF Pro

Simplify regulatory compliance and reporting with our automated PMCF Plan and Report Generators. Stay up-to-date with the latest regulations, reduce operational costs, and ensure high-quality documentation with ease.

AJW Video

Smarter Tools for Post-Market Clinical Follow-Up

Managing PMCF doesn’t have to be a headache. PMCF Pro simplifies your workflow with intuitive planning, automated reporting, and smart data management—so you can focus on what matters: getting and staying compliant in a fast-changing regulatory environment.

medical-device
medical-device
medical-device
medical-device
medical-device
medical-device
bg-grid

PMCF, Simplified

From building your PMCF plan to generating your final report, PMCF Pro helps you handle post market clinical follow-up activities clearly, quickly, and with confidence.

  • Clear, Easy PMCF Management
    Clear, Easy PMCF Management

    Whether you're new to post-market clinical follow-up or a seasoned veteran, PMCF Pro takes the guesswork out of compliance. With tools that reduce errors and streamline collaboration, you'll save time and stay on track.

  • Step-by-Step PMCF Plan Creation
    Step-by-Step PMCF Plan Creation

    Creating a compliant plan can feel overwhelming. We break it down into simple steps based on MDCG 2020-7 and EU MDR requirements. You’ll address every requirement without needing to dig through pages of guidance documents.

  • Simple, Scalable Pricing
    Simple, Scalable Pricing

    Our pricing is straightforward: pay per plan—not per user. That means no surprise fees, and your whole team can collaborate without worrying about licenses. Whether you’re managing one device or a whole portfolio, PMCF Pro scales with you.

  • Quick, Customizable Reports
    Quick, Customizable Reports

    Our report generator turns your plan and data into a structured, regulatory-compliant report—fast. You can include survey responses, literature summaries, and other attachments, all organized into a format that aligns with EU MDR and MDCG 2020-8.

  • Built-In Quality and Consistency
    Built-In Quality and Consistency

    Templates built on EU MDR and MDCG guidance make it easy to create consistent, submission-ready documentation. The system helps reduce mistakes by guiding you through each step and letting you attach supporting files. By auto-populating redundant elements from the plan to the report, PMCF Pro reduces data entry time and the potential for human error and inconsistencies between the documents.

  • Made for Real-World Teams
    Made for Real-World Teams

    PMCF Pro was built with usability in mind—no PhD required. Whether you're in quality, clinical, or regulatory affairs, you’ll find it easy to get started, stay organized, and finish strong.

Recent Articles

Pricing Plans

Choose the right plan for you

Monthly Plan
$95/month

Flexible monthly payments

  • Total $1,140 if paid monthly throughout the year.
  • For early adopters of the platform.
  • Perfect for those starting with minimal commitment.
Annual Plan
$85/month

Upfront payment & Extra savings

  • Total $1,020 annually (Paid upfront).
  • Significant savings for early subscribers.
  • Special rates for early subscribers during the first year.

Free Option for Initial Release

  • Access Limits: To be specified (e.g., limited features, time period)
  • Duration: Free during the product launch phase

Frequently asked questions

Everything you need to know about the product and billing.

Still have questions?

Can’t find the answer you’re looking for? Please chat to our friendly team.


© 2024 AJW Technology Consultants, Inc. All rights reserved.