Traininng.com courses have gained regulatory professionals’ confidence in regulatory issues by addressing pain areas

Fremont, CA: With a section of the most pertinent and value-added courses in the areas of regulatory compliance; Traininng.com has earned the reputation of being a highly accomplished provider of professional trainings that help regulatory professionals address their pain areas.

The rationale for regulatory courses will not be served if they fail to gain the regulatory professionals’ confidence by addressing pain areas, believes Fremont, CA-based provider of professional trainings for all the areas of regulatory compliance, Traininng.com.
Traininng.com is driven by the passion of being a very reliable source of professional trainings for all the areas of regulatory compliance. It wants to be at the forefront of providing professional trainings to professionals with the aim of helping them ease their pain areas. Pain areas are a regular feature that keep cropping up from time to time, even for experienced regulatory professionals, because:
 The regulations keep getting updated from time to time, requiring organizations in the regulated industries to spend considerable resources on implementing them in the exact manner prescribed by the regulatory bodies

 The regulations are sometimes ambiguous and unclear in the wordings or expected outcomes, something that only experienced experts in the field can help to decode and decipher.
Traininng.com’s trainings provide this expert knowledge that help address pain areas for regulatory professionals. By offering hundreds of courses to regulatory professionals in the form of webinars and seminars; Traininng.com is at the forefront of being a highly dependable provider of regulatory trainings. These courses are imparted from some of the best experts in the respective areas of regulatory compliance, which Traininng.com has handpicked for the benefit of its learners.
Many of its experts have worked for regulatory agencies such as the FDA, or have been active members of committees or taskforces that have framed important regulations. This is the kind of repute Traininng.com brings to its courses. It believes that having this kind of pick of experts is the ideal means to help professionals in the regulatory areas address their pain areas.
Traininng.com has empaneled a rich selection of the best experts in the areas in which professionals in the regulated industries need professional trainings. Its panel of experts is a very impressive one. This is just a small sample of the experts who offer professional trainings with Traininng.com:
John N. Zorich quality and compliance for medical devices from new product development, to operations, to post-market activities.: John has spent no fewer than 35 years in the medical device manufacturing industry, during which he has gained expertise in the areas of R&D, Manufacturing, QA/QC, and Regulatory. He has offered his consulting services in the area of statistics to clients ranging from startups to large corporations such as Boston Scientific, Novellus, and Siemens Medical. As an instructor in statistics, he has given hundreds of seminars that have stretched from one hour to three days. The formally-validated statistical application spreadsheets he has created have been purchased by more than 75 companies globally.
Karl J Hemmerich: With more than three decades in medical device product design, development, manufacturing, and sterilization, in which his specialization is sterilization method selection and program development with emphasis on component material selection, process development and sterilization Process Validation; Karl has been a contributing member of the AAMI “Radiation Materials Working Group” that developed Technical Information Report # 17 as the guidance for materials selection, qualification/validation test techniques and quality processing methods for all common sterilization methods. Karl is also a member of the Editorial Advisory Board for MDDI magazine. Not surprisingly, his papers on Radiation Effects on Polymers and General Aging Theory, published in Medical Device and Diagnostics magazine remain industry standards.
Lyn Thomas: Lyn is a very senior and highly respected professional who has his own consulting service in Project management, Business Development, Instrumentation and valves. His clients are located in places as varied as UK, India, Japan and USA. One of the major achievements for Dubai-based Lyn is the valve business he initiated from ground up and developed into a ten-million plus company in a matter of just two years.
Mark Powell: Mark is Director, Mark Powell Scientific Limited, a company he set up with the objective of providing technical support for pre-clinical drug development, which may involve short-term help with specific problems or management of the analytical aspects of a development project, for new or existing compounds, as part of a multi-disciplinary team. Although his areas of expertise are analytical method development and validation (including assay of impurities), design of stability testing studies and auditing of contract laboratories; Mark is also an experienced quality auditor, and can perform GMP audits of contract laboratories, including evaluation of compliance with data integrity requirements.
Susanne Manz: Traininng.com also brings another ace on quality and compliance for medical devices, Susanne Manz, to help address the pain areas and challenges that regulatory professionals could face in the course of their work. Also an auditor for medical devices; Susanne’s expertise emphasizes the areas of quality, compliance, and Six Sigma. She has worked in all the areas of quality and compliance for medical devices from new product deve

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