Having been in the industry for more than three years, we at GlobalCompliancePanel can say with pride and satisfaction that we have successfully completed over 350 training courses, which have benefited more than 15,000 professionals. Over 100 well-versed Experts from various industries, whose collective experience spans many decades, are associated with us.
Our services are aimed at benefitting the Medical Devices, Pharmaceutical, Bio Technology, Food Safety, Financial Accounting Standards, and IT Control & PCI Industries.
Apart from providing excellent training to compliance professionals through compliance and consulting experts, Global Compliance Panelprovides benefits like:
• Information to ensure compliance and enhance quality with regulations for individuals as well as organizations;
• Latest updates on industry trends, industry best practices and any modifications in regulatory affairs;
• An opportunity to share and discuss issues, ideas and best practices, and
• Whitepapers, articles, books on industry standards, training kits, software tools, insights, press releases, etc. on governance, regulatory, compliances and quality management across different industries.
As of December 1, 2011, Global Compliance Panel has conducted two major, highly successful seminars under the series, “FDA India Seminars”. Held in the pharmaceutical hub of India, Mumbai, these seminars were presented by noted Experts on GCP’s panel.
The first of these was titled Guidance on FDA Regulatory Requirements for Indian Pharmaceutical Industry. Well known FDA approvals expert, Dr. Steven Kuwahara conducted this from May 9 to 11. Through this seminar, Global Compliance Panel aimed to familiarise Indian pharmaceutical companies with the nuances of getting FDA approvalfor drugs to the US market.
Attended by over 140 professionals drawn from the top echelons of the Indian pharmaceutical industry, this seminar drove home the point that getting FDA approval for their drugs is not impossible, after all, and that what is need is compliance with the law and some intuitiveness.
The second of these seminars was held on September 15th and 16th. Titled USFDA Seminar, Validation and Part 11 Compliance of Computer Systems, the seminar was conducted by Dr. Ludwig Huber from Lab Compliance, Germany. Attended by over 160 professionals, the seminar was another roaring success. It highlighted the need for Indian pharmaceutical companies to adhere to Validation and Part 11 Compliance of Computer Systems.
It helped participants to get an in-depth understanding about computer system validation understanding and electronic records and signatures. Another aim was to help them receive and understand master plans, step-by-step implementation plan, case studies and fill-in templates to easily develop documents as required by FDA and international agencies.
Global Compliance Panel is an online training solutions provider that delivers high quality compliance and regulatory trainings in an effective, yet simple, cost effective and user friendly format.
Global Compliance Panel offers these trainings through a broad range of highly interactive and interesting channels such as web based training, web alerts and discussion forums.
Global Compliance Panel brings together the regulators or experts on regulation and the learning community which needs to be aware of those regulations.
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GlobalCompliancePanel is an online training gateway delivering high quality regulatory & compliance trainings in a simple, cost effective and in a user friendly format.