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Clinical Research *
Clinical Reporting
Product Development
Real World Data Research
Study Operations & Management
Trial Design & Planning
Commercialization *
Brand Planning & Activation
Customer Engagement
Finance & Investment *
Financial Services
Investment Banking
Market Access & Policy *
Global Market Access
Government Policy
Medical Affairs *
Defining the Value of Medical Affairs
Evidence Generation
Scientific Communications Development
Strategic Communications Planning
Strategic Stakeholder Engagement
Pharmacovigilance *
Risk Management
Safety Systems
Quality & Mfg *
Facilities & Equipment
Production & Supply Chain
Quality Management
Testing & Release
Regulatory *
Compliance
Labeling & Promotions
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Transparency & Disclosure
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Automation & Efficiency
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Digital Health Solutions
Early Development
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Operations
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Greg R.
Heej K. from DIA
Heej K. from DIA
Tong (Jenny) L.
Tong (Jenny) L.
Kindrie E.
Michiel H. from DADA Consultancy B.V.
A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs
Meghann H.
Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of the most strictly controlled industries, more than 50% of product recalls are caused by packaging errors.
Is your company taking all the necessary steps to ensure labeling compliance and accuracy?
Barcode Compliance Guide
Meghann H.
Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive misprints and recalls.
When it comes to grading a digital barcode, there should never be a result other than Pass or Fail – either it is perfect or it is not.
Is your company taking all the necessary steps to ensure that your barcodes scan correctly?
e-Labelling: The Road to Reduced Med Device Packaging
Meghann H.
Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare system by implementing e-labelling initiatives.
The goal of these initiatives is to ensure a sustainable and consistently up-to-date information source for product and safety information that isn’t dependent on paper.
This eBook assesses the latest regulatory expectations and timelines applicable to the medical device industry. It then sets out the practical next steps manufacturers and suppliers can take now – both to prepare for compliance and to maximize the opportunities operationally and for customers.
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