These online courses will continue to be part of our comprehensive course catalog.
Biomanufacturing
Participants will learn the importance and benefits of having and completing Batch Production Records (BPRs) and the differences/similarities/relationship to...
Technical writing is an important part of the life science industry, but only if the reader understands what it is they are reading. Participants will learn...
Aseptic processing is utilized to prevent contamination and manufacture sterile products to ensure patient safety. Contamination of these drug products via the...
Students will learn how to write using the three most commonly needed skills in any type of technical document: writing clearly, concisely, and cohesively. The...
The Bio-Agricultural Program Readiness Opportunity (BioAg PRO) provides practical, hands-on learning and familiarity with cutting-edge techniques,...
All students who complete the BioWork Certificate Program successfully are eligible to take the certification exam.
Students must be able to present...
This course provides an overview of the Food and Drug Administration (FDA) principles, requirements, and expectations for compliance with the Current Good...
This overview of CGMP for Pharma outlines the fundamentals of current Good Manufacturing Practices (CGMP) used by pharmaceutical and biomanufacturing companies...
Aseptic gowning is a system of donning apparel to prevent the contamination of aseptic processing areas. The Cleanroom Gowning course will establish a...
Interactively learn and apply requirements in validating Computer System Applications. By concentrating on information systems and instruction on how to meet...
This course is designed to introduce technicians and professionals to the principles and regulatory requirements of current drug, biologic and medical...
This course introduces principles of contamination and containment for the biopharmaceutical industry along with responses using various procedures and...
Understand the fundamentals of current Good Manufacturing Practices (CGMP) for Biomanufacturing. CGMP exists to protect the health and safety of patients or...
An overview of Good Documentation Practices, including the differences between documents and records, the typical ISO 9001 document hierarchy, and each...
Regulatory authorities are increasingly expecting on-going, competent assessments of internally and externally sourced processes and materials. This course...
This course provides an overview of the concept of validation with a specific focus on EtO sterilization of medical devices. The course addresses why, what,...
FDA Audit Preparation is designed to help create an environment of preparedness to instill a culture of quality assurance by raising the awareness of FDA...
Biomolecules are often the end product and a critical component of the bioprocessing and biopharmaceutical industries. This course provides a basic...
This course is designed to introduce technicians and professionals to the principles and regulatory requirements of current drug, biologic and medical product...
This course is designed to introduce technicians and professionals to the principles and regulatory requirements of current drug, biologic and medical product...
This 24-hour online course covers six modules related to Good Manufacturing Practices (GMP) and effective Standard Operating Procedures (SOP).
Are you responsible for preserving documents or for ensuring that your company’s data is complete and correct?
Stay on top of your field by learning the...
This course presents the regulatory requirements and best practices for medical device documents, documentation, and record keeping. Topics covered will...
This course reviews the regulatory requirements and methods for determining calibration specifications and relates these methods to validation of critical...
This course provides a broad overview of the United States Food and Drug Administration (FDA) principles, requirements, and expectations for compliance with...
A Project Execution Plan (PEP) is much more than a chart showing timescales - it is a document describing how, when, and by whom a specific target or set of...
Quality Risk Management is utilized by companies to determine where the risks lie that may adversely impact the quality of their product and the business...
Take command of your report and learn how to write clear, accurate, and easy-to-read professional records that boost your team’s work.
In our course,...
Students will learn how to write an effective Standard Operating Procedure (SOP) as well as why these are a required and essential component of documentation...
Food, Beverage & Natural Products
Participants will learn the importance and benefits of having and completing Batch Production Records (BPRs) and the differences/similarities/relationship to...
Does your facility produce products with multiple types of allergens? 30% of all recalls stem from problems around allergen labeling. 3rd party audit...
Students will learn how to write using the three most commonly needed skills in any type of technical document: writing clearly, concisely, and cohesively. The...
Does your 3rd party audit certification body require employees to undergo yearly training to meet their specifications? Participation in this refresher...
This course equips food production employees and floor supervisors with all they need to know to stay in compliance with an HACCP system.
As a food safety...
The Current Good Manufacturing Practice, Hazard Analysis, and Risk-based Preventive Controls for Human Food regulation (aka Preventive Controls for Human Food...
Learn to grow probiotic cultures that will aid digestion, preserve foods, and add flavor and nutrition to fruits and vegetables. This course is designed to...
Are you looking to become a Preventive Controls Qualified Individual (PCQI)?
Completing our course is one way to achieve that goal. Developed by the Food...
Keeping food safe for human or animal consumption means knowing how to execute quality safety practices such as personal hygiene, good manufacturing habits,...
Sensory evaluation of food and beverages isn't just for brewers or food scientists! Have you ever wondered what’s going on when you eat something spicy? Why...
Developing or following a Hazard Analysis Critical Control Point (HACCP) plan can be daunting. In this course, learn how HACCP systems work and your role in...
Quality Risk Management is utilized by companies to determine where the risks lie that may adversely impact the quality of their product and the business...
Take command of your report and learn how to write clear, accurate, and easy-to-read professional records that boost your team’s work.
In our course,...
Do you have an amazing herbal product you’d like to share with the world? Then this is the webinar for you! Learn the nuts and bolts of setting up a business...
Students will learn how to write an effective Standard Operating Procedure (SOP) as well as why these are a required and essential component of documentation...