4th Annual ComplianceOnline Medical Device Summit 2021 *** LIMITED TIME OFFER: FREE $100 AMAZON GIFT CARD! *** REGISTER TODAY! Key Attraction Innovate novel ideas for...

HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer With the recent implementation of new HIPAA regulations in the HIPAA Omnibus Update...

FDA's inspection program follows well-established procedures and conducts the inspections with as much consistency as possible. FDA trains its investigators from day one. During...

This 2-Day seminar covers the details of the Regulatory Requirements for a wide-range of Life Science products in Japan: Pharmaceuticals, Biologics, Medical Devices and...

Description The 8th Genomics & Big Data Summit to be held on June 6-7, 2021 in San Diego, CA, has four focus areas to discuss the developments and challenges in the popular...

Overview: Grab a cup of coffee and join us to learn how to analyze the numbers, and use this intel to juice up virtually every facet of your organization's operations from...

Overview: This 60-min webinar will familiarize participants with USP Chapter <1029> on good documentation guidelines. This session will wrap up the general concept and...

A Risk Based Scientific Approach to Analytical Methods Development and Validation Activities for FDA Regulated Industries This Course introduces the schematics of Methods...

Biostatistics for the Non-Statistician Statistics is a useful decision-making tool in the clinical research arena. When working in a field where a p-value can determine the next...

This two-day seminar will begin by laying the foundation for the subject by first defining what a project is and then discussing the unique roles that the project manager must...

On behalf of the organizing committee and global organizations, we take this opportunity to extend a warm welcome to all of you to participate at the 2nd Annual Conference on...

Overview: FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based...

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan Global Medical Device...

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation The European Medicines Agency's (EMA) Guideline on good pharmacovigilance...

Overview: How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions...

Overview: Sponsors or consultants auditing labs on behalf of a pharmaceutical or biopharmaceutical company need strong tools for preparing and conducting audits.Careful...

Overview: The focus will be on drugs, biologics and medical devices, We will also be providing an overview of how the regulatory landscape is currently evolving for most...

Overview: One big issue is how you patrol and control what someone else is saying about your product in a public forum. Once the off-label information is out there, what is...

Nexus 2021 explores how to evolve Nearshore relationships in order to meet the demand for ‘greater intelligence” in all facets of service innovation and delivery. With a proven...

Nexus 2021 explores how to evolve Nearshore relationships in order to meet the demand for ‘greater intelligence” in all facets of service innovation and delivery. With a proven...

Managing Your FDA Inspection: Before, During and After FDA inspects many different kinds of firms. If the FDA regulates your product, they can show up at your lobby and say, “I...

FDA's New Import Program for 2021 - Strict Precision *** LIMITED TIME OFFER: FREE $100 AMAZON GIFT CARD! *** REGISTER TODAY! The FDA continues to change its import program to...

Governance and Change Control according to GxP and GMP Requirements GxP/GMP regulations are required to be used in regulated industries such as food and beverages,...

Since 1979 an International Conference on Magnetic Fluids is held every three years. This conference brings together the international scientific community involved in magnetic...

Background: FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and...

Developing Technical Training in the Life Sciences is a 2-day seminar that addresses the unique challenges of developing and managing training in Life Sciences companies. The...

Prior to developing a process control plan as part of an overall risk management strategy, process development studies must be completed. The objective of these process...

Europe's new Medical Devices Regulation 2020/745 (MDR) takes effect in May-2020. That seems like plenty of time, but smart companies should start planning their CE transition...

Kids Obstacle Challenge is an adventure and obstacle course race series for kids ages 5-16, with 13-15 fun and challenging obstacles and mud! Our mission is to inspire and...

Conferenceseries invites all the participants from all over the world to attend “20th Global Obesity Meeting” during August 20-21, 2020 in Tokyo, Japan which includes prompt...