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31-45 of 76 results
DAN SCUNGIO
$
Dec 26, 2025
02:30 PM
Best Industry Practices - How to Structure and Write a Job Hazard Analysis (JHA) / Activity Hazard Analysis (AHA)
A properly-composed JHA/AHA is one of the primary documents that large clients are increasingly asking to review in advance of allowing you to start work on their Project. The JHA/AHA is not an OSHA requirement however i...
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DAN SCUNGIO
$
Dec 30, 2025
02:00 PM
Best Practices For How To Structure And Write A Standard Operating Procedure (SOP)
Using a library of SOP’s to help organize and control your operations is just good business sense. This is particularly important in high-risk and critical operations, construction or industrial, where a mistake ca...
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MOHAMMAD ELNADI
$
Jan 01, 2026
01:00 PM
Counterfeit Drugs Health, Social & Economic Impact
Counterfeit drugs pose a public health hazard, waste consumer income, and reduce the incentive to engage in research and development and innovation. Stronger state licensure supervision of drug suppliers would be helpful...
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MOHAMMAD ELNADI
$
Jan 01, 2026
01:00 PM
Regulatory Strategy in The Pharmaceutical Industry: Paving the Way From Concept to Commercialization
Regulatory strategy in the pharmaceutical industry refers to the plan put in place by a pharmaceutical company to ensure compliance with laws, regulations, and guidelines set forth by regulatory agencies such as the Food...
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Kelly Thomas
$
Jan 06, 2026
01:00 PM
GMP for QC Laboratory Compliance
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of manufacturing high-quality products. For this reason, every staff member in the pharmaceutical industr...
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MOHAMMAD ELNADI
$
Jan 01, 2026
01:00 PM
Regulatory Policies in Drug Pricing and Reimbursement
The price of medicines is one of the factors that can limit the affordability of medicines to the population.
So there are many drug pricing policies that could be implemented by the regulatory authorities based on the...
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John C. Fetzer
$
Jan 06, 2026
01:00 PM
Analytical Method Validation And Transfe
This course provides guidance on how to perform QC analytical test method validations and transfers. One of the most critical factors in developing and marketing pharmaceutical drug substances and drug products is ensuri...
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MOHAMMAD ELNADI
$
Jan 01, 2026
12:00 PM
Stability Testing Of Pharmaceutical Products From Regulatory Perspective
This webinar gives a fundamental knowledge of stability testing requirements for establishing storage conditions and expiration of pharmaceutical products.
Stability data form an important element of pharmaceutical regu...
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John C. Fetzer
$
Jan 06, 2026
01:00 PM
The Use of Statistical Process Control (SPC) Using Control Charts to Maintain Compliance in the Laboratory
Compliance under GLP can be difficult. The setting up of a system to monitor the performance of methods and instruments can lessen this. Statistical Process Control (SPC) uses control charts and statistical guidelines to...
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John C. Fetzer
$
Jan 06, 2026
01:00 PM
The role of Logbooks and Recordkeeping in Identifying Root Causes
The records in a lab – the logbooks for chemicals, reagents, and calibration solutions, sample preparation, instrument maintenance and calibration, and quality checks – all are time-oriented. This gives a win...
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John C. Fetzer
$
Feb 09, 2026
01:00 PM
Calibration and accuracy under GLP
Accuracy, the ability of a methodology to give results within acceptable limits when compared to known values, is a fundamental and key requirement. Calibration is the most common approach to obtain accuracy.
Accuracy r...
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John C. Fetzer
$
Jan 01, 2026
01:00 PM
Dealing with Bad Data: Errors and Outliers in GLP
Assessment of the cause for non-compliance is a structured series of branching questions. The answers to these eliminate possibilities and eventually highlight a root cause. This process is described, including roles and...
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John C. Fetzer
$
Jan 06, 2026
01:00 PM
Low-level Compound Testing
Low-level compound analysis has many differences from that of the more common analyses aimed at major components. The requirements for accuracy and precision are different. Selectivity to differentiate very similar compo...
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GRAEME LADDS
$
Jan 01, 2026
01:00 PM
Pharmacovigilance Inspections
Regulatory inspections are the end result of the Company QMS assessment. Companies and Sponsors of trials need to have performed audits on all regulatory aspects to ensure compliance before the Regulatory Authorities ass...
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Leon Shargel
$
Jan 01, 2026
01:00 PM
Pharmacokinetics Of Oral Absorption
Participants will be introduced to biopharmaceutic and pharmacokinetic principles that can be applied to systemic drug absorption. Biopharmaceutic processes relate the physical/chemical properties of the drug substance a...
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