MedDeviceSupplyChain.com
Home | About Us | Contact Us | Events | Search | Member Area
INSPECTIONS
How to Prepare for Inspections
Outside US Inspections
Qualified Third Parties
US Inspections
ENFORCEMENT ACTIONS
Consent Decrees
Form 483s
Form 483s News
Recalls News
Warning Letters
Warning Letters News
CAPA
CAPA Essentials
CAPA News
COMPONENT QUALITY
Adulteration
Counterfeiting
DISTRIBUTION
Storage
Tracking
Unique Device Identification
IMPORT CONTROL
US Import Screening
INFORMATION TECHNOLOGY
Data Management
Data Sharing
MANUFACTURING
Auditing
GMPs
Outsourcing
Raw Materials
REGULATIONS/ GUIDANCES/ LEGISLATION
EU
IMDRF/GHTF
ICH
US Regulations
US Regulations News
Other Countries
RISK MANAGEMENT
Product Liability
Risk Assessments
SECURITY AND THEFT
Theft
EU Security Efforts
Non-US Countries
US Security Efforts
SUPPLIER RELATIONS
Acquisitions
Contracts and Agreements
Purchasing Controls
Qualification
Selection and Certification
Home | EU Security Efforts

EU SECURITY EFFORTS
How Far Back Should You Trace the Pedigree of Biologic Starter Materials? EMA Has an Answer for You.
To bolster the heparin supply chain, drugmakers are encouraged to trace supplies of porcine mucosa -- the primary source of crude heparin -- back to the slaughterhouse and provide regulators with the data, a new European Medicines Agency (EMA) draft document states. . . . more
EC Draft Guideline Tightens Supply Chain Requirements
The European Commission (EC) is tightening supply chain guidelines, requiring pharmaceutical distributors to audit and approve transportation hubs where the products are loaded and reloaded. . . . more
Home | Search | Contact Us | Tell a Friend

© 2013 MedDeviceSupplyChain.com All Rights Reserved. Reproduction without permission prohibited.
This site is powered by MemberGate Membership Site Software