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Pharmaceutical / Medicinal
MAR
3
Managing GMP Compliance and Phase Appropriate GMP Considerations for Virtual Companies This program combines general considerations for Good Manufacturing Practice (GMP) compliance management with the principles of phase-appropriate GMP considerations, with an emphasis on needs of virtual companies. (“Virtual companies” are those wh...
03 - 04 Mar 2026
Online Event | United States
MAR
10
BPS
9th Annual Bioprocessing Summit Europe Bioprocessing Summit Europe brings together 650+ professionals from industry and academia, along with 60+ exhibitors, to advance the manufacture, quality, and control of cutting-edge biologics, genetic therapies, peptides, and oligonucleotides. ...
10 - 12 Mar 2026
Barcelona, Spain
MAR
11
40th Pharmacovigilance UK & EU 2026 40th Pharmacovigilance UK & EU 2026 11 & 12 March 2026, Sheraton Skyline, Heathrow, London, UK This event will bring together top pharmaceutical, biotechnology and regulatory representatives under one roof that will address the key issues of the...
11 - 12 Mar 2026
Hayes, United Kingdom
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

Apr
18

SOP Writing, Training and Compliance in the Pharmaceutical Industry

 
 Seminar/trade show (noCPF)

When:

  18 Apr 2022 through 19 Apr 2022

Where:

  Online Event | United States

Website URL:

  https://www.complianceonline.com/sop-writing-in-pharma-gmp-environment-seminar-training-80560SEM-prdsm?channel=Brownwalker

Sponsoring organization:

  Compliance Online

Categories:

  Medicine & Health - Pharmaceutical / Medicinal

Keywords:


Event description:

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood the extent of the commitments we make when we write an SOP or how the writing of the SOP can have a positive or negative impact on training or job performance. For example, there is an expectation that procedures describe the most critical processes for product manufacturing and will be followed consistently, with few if any deviations. In this course you will learn the keys to writing effective SOPs, the vital connection between the documentation and training spheres, and how to maximize this connection to improve the quality of both SOPs and training. To accomplish these goals, we will review regulatory agency expectations when an SOP is written, provide suggestions for uncovering the process in its entirety and describe it clearly and concisely, indicate how to break portions of the process... Read more

Posting date:

06 March 2022  |  537 views

Placement:

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