Upcoming Events
Pharmaceutical / Medicinal
MAR
17
Verification and Validation - Product, Equipment/Process, Software and QMS Develop / review a company's Master Validation Plan for major cGMP deficiencies. Address the U.S. FDA's newer and tougher regulatory stance. One major failing is lack of sufficient or targeted risk-based V&V planning: Start with a Master Va...
17 - 18 Mar 2026
Online Event | United States
MAR
18
OPTC
OPT Congress 2026 OPT Congress 2026 is the leading industry event for scientists, directors, and technology providers driving innovation across oligonucleotide, mRNA, and peptide therapeutics. Now in its 11th year, this event provides a unique forum for translating...
18 - 19 Mar 2026
Boston, United States
MAR
19
SOP Writing, Training and Compliance in the Pharmaceutical Industry Recording of Live Virtual Seminar conducted on June 19-20, 2025 Complete this training at your own pace within 5 working days. The recording will be enabled on your convenient dates. Standard Operating Procedures (SOPs) are the basis for a lar...
19 - 20 Mar 2026
Online Event | United States
MAR
23
Change Control Best Practices - Avoiding Unintended Consequences of Changes One of the top 10 FDA 483 and Warning Letter citations is for inadequate change control. Change control receives detailed scrutiny during FDA inspections, and FDA reviews change control documentation to determine that changes did not adversely imp...
23 - 24 Mar 2026
Online Event | United States
MAR
24
VIPRY 2026
9th Annual Pharma Regulatory Summit 2026 9TH ANNUAL PHARMA REGULATORY SUMMIT 2026 “Driving Regulatory Excellence for a Changing Pharma Landscape” 24th March 2026, Hotel Kohinoor Continental, Mumbai, India The 9th Annual Pharma Regulatory Summit 2026 congregates foremost globa...
24 - 24 Mar 2026
Mumbai, India
MAR
26
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms an...
26 - 27 Mar 2026
Online Event | United States
MAR
31
23rd Annual Strategic Alliance Management Congress As biopharmaceutical innovation becomes more collaborative and global, effective alliance management increasingly plays a decisive, business-critical role—transforming partnerships into powerful engines of progress. Now in its 23rd year &nda...
31 - 01 Apr 2026
Boston, United States
APR
16
Good Manufacturing Practices (GMP) Good Manufacturing Practices (GMP) describe the requirements for manufacturing drug product in each country or region and cover areas such as facility design and sanitation, product testing, product identification, equipment, packaging, warehousin...
16 - 17 Apr 2026
Online Event | United States

Feb
10

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

 
 Seminar/trade show (noCPF)

When:

  10 Feb 2026

CFP Deadline:

  06 Feb 2026

Where:

  Online Event | United States

Website URL:

  https://www.complianceonline.com/understanding-reach-and-rohs-compliance-protecting-revenues-with-advanced-compliance-seminar-training-80668SEM-prdsm?channel=Brownwalker

Sponsoring organization:

  Compliance Online

Categories:

  Engineering & Technology - Pharmaceutical / Medicinal

Keywords:


Event description:

This one day virtual seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others. We will review the latest on both directives and will draw out key developments and key dates (if applicable) with particular emphasis on requirements for US firms. Learning Objectives: After completing this seminar, you will gain a better understanding of: Understanding your organization’s liability under RoHS and REACH. Review case studies. Discuss lessons learned applications to ensure full compliance. RoHS and REACH guidelines REACH Registration of Substances Introduction to REACH Articles and REACH Substances of Very High Concerns (SVHC) Supply chain communication Compliance enforcement Basics of RoHS Background and content of RoHS Responsibility for RoHS International requirements of RoHS WEEE - background and content of WEEE and how to work to meet requiremen... Read more

Posting date:

11 April 2022  |  599 views

Placement:

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