5 November 2020
11 November 2020

6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

12 November 2020

4-Hour Virtual Seminar on Transformational Leadership - The Ultimate Leadership Course

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

16 November 2020

6-Hour Virtual Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times. Beginning in May 2017, the eCTD will be required in the US for all marketing applications.

16 November 2020

6-Hour Virtual Seminar on Applying ISO14971 and IEC62304 - A guide to practical Risk Management

Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible.

17 November 2020

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

17 November 2020

6-Hour Virtual Seminar on Phase I GMPs

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy

17 November 2020

6-Hour Virtual Seminar - HIPAA - Emailing, Texting, and Personal Devices (myths vs realities)

This six-hour seminar will be going into great detail regarding you practice or business information technology and how it relates to

17 November 2020

6-Hour Virtual Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems

This course is appropriate for beginner and experienced person alike.

17 November 2020

6-Hour Virtual Seminar on How to be HIPAA Compliant

This 6-hour webinar takes the participants through HIPAA compliance from start to compliance.

17 November 2020

6-Hour Virtual Seminar on Master Class for the HIPAA Officer: Protecting Patient Information and Implementing Today's Privacy, Security, and Breach Regulations

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

19 November 2020

6-Hour Virtual Seminar on Effective Complaint Handling and Medical Device Reporting

Complaint Handling and Medical Device Reporting (MDR) are a part series on Post Market Compliance

19 November 2020

6-Hour Virtual Seminar on Moving From An Operational Manager to A Strategic Leader

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

19 November 2020

6-Hour Virtual Seminar on Effective Technical Writing in the Life Sciences

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

20 November 2020

6-Hour Virtual Seminar on Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable.

20 November 2020

6-Hour Virtual Seminar on HIPAA Training for Compliance Officer

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house

20 November 2020

6-Hour Virtual Seminar - Medical Claims Boot Camp - Cracking the Code to Healthcare Billing, Coding and Reimbursement

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

20 November 2020

6-Hour Virtual Seminar on Stress Management & Burnout Prevention in the Workplace: Strategies & Solutions

Professionals are under more stress than ever evidenced by increases in demand for better services that are more efficient.

20 November 2020

6-Hour Virtual Seminar on Toxic Work Behaviors Erode the Patient Experience (More Than You May Know!)

We can no longer stand by and let toxic people erode patient safety, our self-esteem, and the bottom line! This webinar will help you take immediate action!

23 November 2020

6-Hour Virtual Seminar on SOP Writing, Training and Compliance in the Pharmaceutical Industry

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

23 November 2020

6-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

23 November 2020

6-Hour Virtual Seminar on A Risk Based Approach To Data Integrity

This course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system

24 November 2020

6-Hour Virtual Seminar - Batch Record Review and Product Release

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

24 November 2020

6-Hour Virtual Seminar on HR Compliance 101 - for Non HR Managers

Knowing what to do in employee situations can be difficult for even seasoned Managers and Supervisors, especially if a Supervisor has never had training.

24 November 2020

6-Hour Virtual Seminar on HIPAA vs. SAMHSA 42 CFR Part 2

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

25 November 2020
25 November 2020

6-Hour Virtual Seminar on The Interplay of the Americans With Disabilities Act, the Family and Medical Leave Act, and Workers' Compensation

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

25 November 2020

6-Hour Virtual Seminar on Transition from Peer to Supervisor

Today's workforce is experiencing high turnover and disengaged employees.

30 November 2020

6-Hour Virtual Seminar on Combination Products

This seminar provides Professionals working in this area with:

6-Hour Virtual Seminar on Moving From An Operational Manager to A Strategic Leader (Including Remotely)

Gain the insights and skills to know where your business stands today and where it’s heading tomorrow.

  • View Anytime
  • Duration: 6 Hours
  • Price: $595.00
  • View Details

6-Hour Virtual Seminar on The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future

One of our most popular webinars, continuously updated with the latest U.S. FDA and Eurpean Union requirements.

  • View Anytime
  • Duration: 6 Hours
  • Price: $595.00
  • View Details

6-Hour Virtual Seminar on HIPAA Training for Compliance Officer

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Effective Technical Writing in the Life Sciences

This webinar will begin with a general discussion of technical writing and its role within the life sciences.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Master's Program for the HIPAA Compliance Officer: Safeguarding Patient data and Implementing Privacy, Security, and Breach Regulations - 2020 update

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

4-Hour Virtual Seminar on Transformational Leadership - Discover The Techniques Of The World’s Greatest Leaders

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

  • View Anytime
  • Duration: 4 Hours
  • Price: $395.00
  • View Details

6-Hour Virtual Seminar on Statistical Process Control & Process Capability

Statistical Process Control charts have been called the Voice of the Process.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Combination Products

This seminar provides Professionals working in this area with:

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on HIPAA vs. SAMHSA 42 CFR Part 2

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Controlling Human Error in the Manufacturing Floor

Human error is known to be the primary cause of quality and production losses in many industries.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited. The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times. Beginning in May 2017, the eCTD will be required in the US for all marketing applications.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Applying ISO14971 and IEC62304 - A guide to practical Risk Management

Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Phase I GMPs

Early clinical trials are conducted to establish initial safety of a drug.The studies are generally in small number of healthy

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar - Batch Record Review and Product Release

Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar - HIPAA - Emailing, Texting, and Personal Devices (myths vs realities)

This six-hour seminar will be going into great detail regarding you practice or business information technology and how it relates to

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on SOP Writing, Training and Compliance in the Pharmaceutical Industry

Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement

Upon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on HIPAA Training for Compliance Officer

This 6-hour seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems

This course is appropriate for beginner and experienced person alike.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on A Risk Based Approach To Data Integrity

This course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar - Medical Claims Boot Camp - Cracking the Code to Healthcare Billing, Coding and Reimbursement

This course covers the fundamentals of medical billing, coding, and reimbursement by explaining how all of these components work together. Emphasis will be placed on the practical application of the latest industry knowledge and standards, with the goal of helping those who work with medical claims and claims data stay ahead of the game.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Stress Management & Burnout Prevention in the Workplace: Strategies & Solutions

Professionals are under more stress than ever evidenced by increases in demand for better services that are more efficient.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on How to be HIPAA Compliant

This 6-hour webinar takes the participants through HIPAA compliance from start to compliance.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on The Interplay of the Americans With Disabilities Act, the Family and Medical Leave Act, and Workers' Compensation

The Americans with Disabilities Act (ADA) prohibits discrimination against applicants and employees who are "qualified individuals with a disability."

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Toxic Work Behaviors Erode the Patient Experience (More Than You May Know!)

We can no longer stand by and let toxic people erode patient safety, our self-esteem, and the bottom line! This webinar will help you take immediate action!

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Master Class for the HIPAA Officer: Protecting Patient Information and Implementing Today's Privacy, Security, and Breach Regulations

The session begins with overview of the HIPAA regulations and then continues with presentation of the specifics of the Privacy Rule

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Transition from Peer to Supervisor

Today's workforce is experiencing high turnover and disengaged employees.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Moving From An Operational Manager to A Strategic Leader

Gain the insights and skills to know where your business stands today and where it's heading tomorrow.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Effective Technical Writing in the Life Sciences

This seminar will begin with a general discussion of technical writing and its role within the life sciences.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on HIPAA vs. SAMHSA 42 CFR Part 2

This 6-hour seminar will cover the latest SAMHSA and HIPAA updates which were released in January 2018 and December

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Payroll Virtual Boot Camp: Wage & Hour

This webinar concentrates on five areas of wage and hour law:

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

4-Hour Virtual Seminar on Transformational Leadership - The Ultimate Leadership Course

The Bulk Of What Is Being Taught About Leadership In Universities Today Is Based On Old B.S. (“Belief Systems”).

  • View Anytime
  • Duration: 4 Hours
  • Price: $395.00
  • View Details

6-Hour Virtual Seminar on Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable.

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details

6-Hour Virtual Seminar on Effective Complaint Handling and Medical Device Reporting

Complaint Handling and Medical Device Reporting (MDR) are a part series on Post Market Compliance

  • View Anytime
  • Duration: 6 Hours
  • Price: $495.00
  • View Details