Description The secret to preventing medical device recalls is to implement and follow basic practices for specifications and design control, design for process reliability,...

Moving Day Boston October 14, 2020 DCR Artesani Park Boston 9:30am Moving Day is more than just a walk. It highlights movement and exercise as symbols of hope and progress...

Overview: A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of...

Overview This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable...

Overview This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable...

Overciew This seminar will explore the best practices and strategic approach for evaluating computer systems used in the conduct of clinical trials and determining the level of...

DESCRIPTION BOSTON EVENT PLANNING CERTIFICATE PROGRAM October 14-15, 2020 1:00 PM – 4:00 PM each day DoubleTree 400 Soldiers Field Road, Boston, MA 02134 Registration Fee $375...

Overciew This seminar will explore the best practices and strategic approach for evaluating computer systems used in the conduct of clinical trials and determining the level of...

Join She+ Geeks Out and Drizly for happy hour at their beautiful offices in Boston! Expect wonderful company, delicious food and drinks. We’re looking forward to seeing you for...

Calling all tech enthusiasts and geeks - getgeeked is coming to Boston on October 13th! getgeeked Boston is an exclusive showcase featuring innovative technology companies from...

Join us for Sustainable Business Network’s 2nd Local Craft Spirits Festival on Friday, October 13th, 2020, 6:30 (6:00pm VIP) - 9:30 PM in Kendall Square, Cambridge, MA. Back by...

A biopharma company’s very survival depends on its ability to maintain product quality throughout every step of clinical and commercial manufacturing. You must always be...

As the growth of the sensors market continues to rapidly expand, Sensors Midwest will bring together thousands of engineers in the Midwest marketplace looking for access to the...

What you'll learn? Understand the Rules Review Rule Definitions Plan label change implementation immediately Compliance with mandatory deadlines based on company size Know your...

What you'll learn? Understand the Rules Review Rule Definitions Plan label change implementation immediately Compliance with mandatory deadlines based on company size Know your...

FDA Field Inspectors conduct administrative and enforcement activities related to the Quality System (QS) Regulation (21 CFR 820), the Medical Device Reporting (MDR) Regulation...

Topics include: Antibacterial Discovery & Development, Targeting Gram-Negative Pathogens, and Short Courses. Event is designed as a knowledge and experience exchange for the...

We are witnessing rapidly unfolding efforts to reinvigorate the antibacterial pipeline, improve antimicrobial stewardship and bring the multidrug microbial resistance under...

> 12th annual FX Invest North America conference > The leading foreign exchange buy-side meeting for institutional investors, asset managers, corporates, pension funds and...

The Microbiome Movement - Drug Development Summit continues to be the industry-leading forum to help forward thinking researchers from the pharmaceutical, biotech and academic...

Overview: This webinar will describe a system, based on the regulations and practical experience that will allow for efficient control of the change process. It will be...

Overview: In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process...

Overview: The single most important element of medical device risk management is the Risk Management Plan (RMP). It ranges from Top Management's risk policy to review and...

Session Highlights • The 21st Century Cures Act • New processes for expediting drug and medical device approval for new products and new product indications • How to prepare for...

The International Standards Organization (ISO) defined the ISO 26000 guideline for the use and planning of all structured, measures, and monitored social responsibility...

Description This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products to your customers....

Texting and E-mail with Patients Under HIPAA — Meeting Patient Rights and Avoiding Breaches Tuesday, October 17, 2020 from 1:00 PM to 2:30 PM (EDT) This session will focus on...

Live Webinar DHF, DMR, DHR, and Technical File / Design Dossier – And the New EU MDR” October 17, 2020 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 90 Minutes Description...

FDA Focus:Purchasing / Supplier Controls for Medical Devices Overview This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to...

Session Highlights • The 21st Century Cures Act • New processes for expediting drug and medical device approval for new products and new product indications • How to prepare for...