"Keys to an Effective Technology Transfer as an Element of the Knowledge Management Requirements from ICH Q10" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 21.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on March 20 on the topic, "Global Medical Device Adverse Event Reporting Systems in EU, Canada and US". Dr. David Lim, a certified RAC and Certified Quality Auditor (CQA), will be the speaker at this webinar.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Japan -Regulatory Filing Requirements and Compliance Processes for Life Sciences" on March 20.
"Meet the U.S. FDA's Tougher Requirements for the 510(K)" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 20.
A RAPS pre-approved webinar on the topic, "Good Documentation Practices for GMP Operations" is being organized by GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, on March 19. This webinar earns up to 1.00 RAC credits towards a participant's RAC recertification upon full completion.
Future growth in the developed healthcare markets is expected to be buffeted by a massive wave of patent expirations coupled by numerous cost constraining measures.
A RAPS pre-approved webinar on the topic, "Project Management for Computer Systems Validation" is being organized by GlobalCompliancePanel, a leading provider of regulatory and compliance continuing education training, on March 14.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organizea RAPS pre-approved webinaron the topic, "Managing Your Medical Device Reporting (MDR) Program for Compliance Success",on March 13.
"Medical Device Adverse Event Reporting Systems in EU, Canada and US" is the topic of a RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on March 6. This webinar, a 60-minute session, earns 1.00 RAC credits towards a participant's RAC recertification upon full completion.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Disinfection and Clean room Cleaning in an FDA Regulated Environment" on March 5, 2013.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Complaint Handling in Compliance with FDA and ISO Regulations" on March 5. This 60-minute webinar earns up to 1.0 RAC credits towards a participant's RAC recertification upon full completion.
IndustryMonitor.co Publishes Global Pharmaceutical Survey 2013-2014 - Market Trends, Buyer Spend and Procurement Strategies in the Global Pharmaceutical Industry.
"Combination products" is a broad term. The FDA describes it in fairly straightforward terms thus: "Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products." Although simple in description, the complexity lies in the fact that there are very many combinations in the market, and they all have to be regulated.
Steven Walfish, President of Statistical Outsourcing Services will be the Speaker ata RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organizeon February 19, 2013. It will be on the topic, "Using Statistics to Determine Sample Size" .
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Outsourcing Management -Effective Contract Manufacturers, Supplier Evaluation, Approval and Monitoring", on February 21. Miguel Montalvo, President of Expert Validation Consulting, will be the speaker at this 90-minute webinar.
The Larvol Group, LLC announced today that it will provide a preview of its free pharmaceutical intelligence online platform, Larvol Sigma, on February 19th at the Pharma CI Conference in Zurich, Switzerland.
Good Automated Manufacturing Process (GAMP) 5 is a set of five important principles of automated manufacturing processes in the field of Life Sciences. Since it provides practical industry guidance on how to achieve compliant systems fit for intended use; it is considered the "how to" of a validated system in this industry.
GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, "Good Laboratory Practice Regulations -Introduction and Strategies for Implementation" on March 21 and 22 at Mumbai, India.
"Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process" is the topic ofa RAPS pre-approved webinar that GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize on February 13.
In the course of his discussion, the presenter, David Nettleton will demystify Part 11 and the new European equivalent Annex 11. This session will put participants on the right track for using electronic records and signatures, which will help them to greatly increase productivity.
GlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, "Design of Experiments and Statistical Process Control for Process Development and Validation" on February 7 and 8 at Orange County, CA.
Many problems have arisen in the past when designing and scaling-up lyophilization cycles because this process was subjective, being more of an art than a science, and cycles were designed and scaled-up based on a "trial and error" approach.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, "Clean room Design, Certification & Validation" on February 7, 2013. This 75-minute webinar earns up to 1.25 RAC credits towards a participant's RAC recertification upon full completion.
Adaptive clinical trials, owing to their flexibility, help bring in the latest technological findings midway through into a clinical trial. This helps improve the end result quite dramatically.
GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize RAPS pre-approved webinar on the topic, "510(K): Format and Contents", on , February 6.Dr. David Lim, a certified RAC and Certified Quality Auditor (CQA), will be the speaker at this webinar, which earns up to 1.00 RAC credits towards a participant's RAC recertification upon completion.
iPoint Mobile CRM continues to be the first choice for pharmaceutical companies looking to put the iPad in the hands of their reps. iPoint is the most customizable mobile CRM that meets PDMA compliance anywhere.
New Market Research Report Added In MarketResearchReports.Biz Database Cytomegalovirus (CMV) Infections - Pipeline Assessment and Market Forecasts to 2019.
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