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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
The Federal False Claims Act: Enforcement and Recent Updates
The session will provide an overview of the Federal Civil False Claims Act (FCA) and how it works. It will also provide an assessment of enforcement activities, showing how healthcare providers may be at risk. In addition, the session will review recent cases ...
- Basic & Intermediate
- 60 Mins
- William Mack Co
- Mar 31, 2023
Validation Sampling Plans
This webinar will discuss setting up statistically justified sampling plans for process validation. Discussion will also involve using the sampling plan to set acceptance criteria for process validation. Setting acceptance criteria for test method validation w ...
- Intermediate
- 60 Mins
- Alan M Golden
- Apr 07, 2023
The Anti-Kickback Statute: 2022 – Year in Review
The AKS is currently the focus of law enforcement officials. The Statute provides that the offer or payment, as well as the solicitation or receipt, of “any remuneration” in exchange for referrals of any good, facility, service, or item for which payment may b ...
- Basic & Intermediate
- 60 Mins
- William Mack Co
- Apr 12, 2023
HOW TO BECOME HIPAA COMPLIANT
The primary goal of this session is to demonstrate why the health care organization needs to be HIPAA compliant and the steps necessary for meet the HIPAA regulations. This includes a description of the HIPAA Privacy and Security Regulations, definitions of k ...
- Basic
- 60 Mins
- James Wener
- Apr 13, 2023
Implementing a Robust Supplier Management Program
Regulatory expectations are clear about manufactures’ responsibility regarding supplier quality oversight. All regulatory agencies agree that pharmaceutical and medical device manufactures are responsible for ensuring their suppliers adhere to quality standar ...
- Basic & Intermediate
- 90 Mins
- Kelly Thomas
- Apr 19, 2023
HOW TO RESPOND TO A HIPAA BREACH
Participants will review what a HIPAA breach is and what to do when a HIPAA breach occurs. This includes determining if the disclosure of patient health information was a breach or wasn’t a breach. The participants will learn what to do if the breach occurred ...
- Basic
- 60 Mins
- James Wener
- Apr 27, 2023
Implementing a Robust Change Control Program
Regulatory agencies require pharmaceutical and medical device companies to have a systematic approach to managing all changes made to a facility, their product or a quality system. Given the fact that changes are inevitable, it is essential that companies hav ...
- Basic & Intermediate
- 90 Mins
- Kelly Thomas
- May 01, 2023
Fundamentals of CIP, CDD, EDD, CTR, and Current Issues
During this webinar, we will go over the of fundamentals of CIP, CDD, EDD, CTR and also, current Issues that impact your day to day.
- Basic & Intermediate
- 60 Mins
- Justin Muscolin
- May 05, 2023
THE ROLE OF IT IN HIPAA COMPLIANCE
The purpose of this presentation is to help the health care organization structure its HIPAA compliance program in a way that allows the allows IT to be a constructive part of the HIPAA compliance effort. This includes understanding that implementing basic IT ...
- Basic
- 60 Mins
- James Wener
- May 15, 2023