Search Trainings
COST/PRICE ANALYSIS IN PROCUREMENT
When organizations discovered they needed to lower costs, the purchasing people would frequently go to suppliers and demand cost reductions. Now, professionals recognize that bullying their suppliers might provide a one-time, quick fix on the price, but it ...
- Basic & Intermediate
- 75 Mins
- Michael Gozzo
- Mar 21, 2023
How to get a 510(k) for a Machine Learning Product
We will explain what a 510(k) is and explain the other FDA regulatory pathways. We will discuss how software can be considered a device by the FDA. The procedure to obtain a 510(k) will be explained. The contents of the submission to the FDA will be explain ...
- Basic & Intermediate
- 60 Mins
- Edwin Waldbusse
- Mar 23, 2023
The 6 Most Common Problems in FDA Software Validation and Verification
This training on FDA software validation and verification will provide you with the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.
- Basic & Intermediate
- 120 Mins
- David Nettleton
- Mar 23, 2023
Medical Device Software Validation Meeting FDA Regulations
This course will teach how to conduct a software validation program for medical devices containing software that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are us ...
- Basic & Intermediate
- 60 Mins
- Edwin Waldbusse
- Mar 28, 2023
Introduction into Discrete event simulation methodology (DES). Part 1. Dynamic supply & demand balance and capacity problems
Discrete event simulation (DES) is the most powerful methodology used in process data analytics. The following examples will be covered: (i) Outpatient clinic: centralized or separate locations? (ii) Outpatient clinic: non-steady-state operations, (iii) Outpa ...
- Basic & Intermediate
- 90 Mins
- Alexander Kolke
- Mar 30, 2023
Current GXP expectations on Water system validation compliance
The most crucial factor to achieve Business Growth in Pharma manufacturing nowadays, is Compliance with GMP norms, so as to increase the technical and financial strength of Manufacturing units. Currently, the aspect focused on by most Auditors, both internal, ...
- Basic & Intermediate
- 90 Mins
- Hitendra Kumar
- Mar 31, 2023
GMP overview for QC Laboratories
In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect for manufacturing high-quality products. For this reason, every staff member in the pharmaceutical industry has to be familiar with the basic GMP ...
- Basic & Intermediate
- 90 Mins
- Kelly Thomas
- Apr 03, 2023
INVENTORY PLANNING, MANAGEMENT & CONTROL
Today’s economics in business has brought many companies to address major investments like inventory with a limited results solution of outsourcing the function and/or activity. Procurement Services & Contract Manufacturing activities are typically what has ...
- Basic & Intermediate
- 75 Mins
- Michael Gozzo
- Apr 04, 2023
Biomarkers in Drug Discovery and Development
Biomarkers are a key medical product development tool capable of facilitating the development of medical products and spurring innovation. When used in the right context, biomarkers have the potential to help expedite patient access to safe and effective treat ...
- Basic & Intermediate
- 60 Mins
- Stefano Persian
- Apr 05, 2023
Investigating OOS results
This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor, and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the step ...
- Basic & Intermediate
- 60 Mins
- Danielle Delucy
- Apr 06, 2023