Attend the Best GLP Training With the Industry Leaders!

GLP, the abbreviation of ‘Good Laboratory Practice’ stands for the standard or accepted practices that need to be a part of any laboratory that professionals use for scientific analysis, testing, and assessment. The trainees attending the GLP training courses must know about the good practices that are a part of any laboratory where they plan, perform, monitor, record, and report environmental safety and non-clinical health studies.

The GLP Training

GLP training is indispensable for the companies that are involved in the manufacture of industrial chemicals, veterinary drugs, pharmaceutical products, pesticides, cosmetics, and feed and food flavors. As these businesses require to maintain superior standards conforming to the FDA norms, conferring the best GLP training to the professionals becomes 100% necessary.

Good Laboratory Practices applied in a company safeguard high-quality data testing. It also promises the quality and dependability of the workroom with regard to data study integrity, data traceability, and investigation.

Get GLP Training from the Professionals!

World Compliance Seminars (WCS) is sure to be the most dependable answer to your question of ‘where can you get the best quality of GLP training and get the certification?’ We have been offering one-stop solutions for life-sciences training. It provides an in-depth, up-to-date, and most thorough understanding of how the EMA and FDA work internally. The knowledge gained through the WCS training programs can alter the manufacturing and development strategies of companies.

World Compliance Seminars (WCS) suggest training through meetings taken by knowledgeable instructors, virtual seminars, webinars, interactions, and examples. The seminars or sessions are in accordance with the U.S. Food and Drug Administration regulations.

Benefits to the Organizations With GLP Training!

Organizations or Businesses associated with laboratory testing and evaluation can get some substantial benefits from GLP training. They can take on-site training, which recruits better knowledge and application practices. After the conclusion of the course, the participants would surely know about the basics of the GLP training as per the Organization for Economic Co-operation and Development (OECD).

Content of the Course

This two-day GLP training session that World Compliance Seminars offers, includes the basics of the FDA laws and regulations for Quality Control (QC) laboratories. It includes subjects include the following:

▪         What is contamination?

▪         Laboratory organization or formation

▪         Record-keeping and documentation requirements

▪         Sample integrity requirements

▪         Stability studies

▪         Analytical methods validation and verification

▪         Control and management of laboratory instruments

▪         Control and management of laboratory supplies

▪         Conducting laboratory investigations

▪         Laboratory non-compliance consequences

Who Should Attend Good Laboratory Practice (GLP) Training?

Experts recommend GLP training courses must be attended by all the professionals working in various manufacturing units and companies involved in the testing and analysis of health products. These service providers are directly or indirectly used by the customers.

The GLP training and certification program must be joined by supervisors, managers, and senior-level directors who shoulder the duties and responsibilities to maintain the standards of Quality Control labs. It is believed that the training session must be attended by science graduates and university students that intend to take up laboratory testing careers later on. When the GLP is implemented, it is assumed that the company follows high manufacturing standards which assure high-quality products. Therefore, GLP training helps in:

▪         Quality control

▪         Quality assurance

▪         Research & development

World Compliance Seminars (WCS) is one of the leading platforms that offer high-quality certification programs for companies involved in biotechnology, medical devices, and pharmaceuticals.