Blog
Choosing the right promotional material review system
This article provides a comprehensive framework for evaluating pharmaceutical regulatory compliance software vendors specialising in promotional material review systems.
The Billion-dollar risk: Why pharma needs document review to avoid compliance catastrophes.
"The Billion-Dollar Risk" explores how inadequate document review practices can lead to regulatory scrutiny and fines.
From snail mail to streamlined approval review cycles
How to accelerate your promotional materials review and approval process.
Is your pharma marketing compliant? The Audit Trail will tell
This article discusses the importance of Audit Trails in pharma software systems
The ultimate business case for document review and approval systems in the pharmaceutical industry
This article provides a detailed framework for generating a business case for document review and approval systems.
Marketing brilliance without breaking the rules: Pharma's balancing act.
How pharmaceutical companies can balance creative marketing and regulatory compliance.
Unlocking the potential of AI: A Practical Guide for implementing AI in the pharmaceutical industry
Implementing generative AI solutions for efficiency and compliance.
Decoding AI:Black-Box Models and Hallucination Risks
Implementing generative AI solutions for efficiency and compliance.
The GDPR playbook for Pharma: Compliance, Challenges, and Solutions
A comprehensive guide to navigating GDPR requirements for pharmaceutical companies.
Drowning in paperwork? How to escape your promotional material review nightmare
A guide to optimising review and approval processes in the pharmaceutical industry.
AI transparency in Pharma: Meeting the EU AI Act's demands
Opportunities and challenges for using AI in pharmaceutical industry.
Streamlining pharma promo review processes: Mastering the shift to digital review
Transitioning from manual to digital promotional material review in the pharmaceutical industry
CASE STUDY: Streamlining pharmaceutical document approvals in Australia with ApprovalFlow
This article explores how ApprovalFlow transformed a leading Australian pharmaceutical company's document and promotional material review processes.
Securing pharmaceutical document systems: A best-practice guide.
Key requirements for securing document approval systems in the pharmaceutical industry.
CASE STUDY: Bridging borders with ApprovalFlow
Enhancing cross-region collaboration and compliance in pharma, across Europe and the US.
Mastering the Transition: Change Management for Medical, Legal Review (MLR) systems in the pharmaceutical industry
This article discusses best-practice guidelines to implement digital MLR systems.
Ensuring trust and compliance: A guide to software validation in the pharmaceutical industry
Demystify software validation software systems within the pharmaceutical industry.
Mastering compliance: Why the ABPI Code of practice matters more than ever
A how-to-guide on navigating the complexities of the ABPI Code.
Promotional Material Review Systems: Alignment with the ABPI Code
Best practices for building an effective, compliant PMR system
Disaster Recovery Plans: How to safeguard your data and minimise downtime
A best-practice guide to developing a DRP
Email chaos: How manual, email-based workflows are a massive compliance risk
A case for using structured online approval systems
Exploring the European Medicines Agency (EMA): The EMA’s role in promotional material review
Overview of the EMA guidelines for promo review
Understanding the EMA and ABPI: Comparison, overlap, and best practices for promotional compliance
Navigating the complexities of the EMA and ABPI
Why the delete button doesn't exist in pharma: A compliance imperative
A guide to 21 CFR Part 11
When regulators come knocking: Ensuring compliance of your promotional material review system
Data retention requirements in regulated environments
Medical vs. Regulatory Review Understanding the critical differences
Promotional Material Review implications
Medical Review A Practical Guide
Promotional Material Review implications
AI in Pharma Protecting sensitive patient data
Fortifying pharmaceutical innovation when using AI
Regulatory Affairs The importance of this role in promotional material review
A strategic guardian in the review process
Trust & truth in healthcare The power of Medical & Regulatory review
A strategic guardian in the review process
Audit-Readiness How to prepare for a promotional material audit
A detailed guide to help you prepare