20 MCQs on Good Laboratory Practice, Roll 73, 7th Sem, A

GLP is an official regulation that was created by the FDA

• 1977

• 1978

• 1979

• 1980

Full form of OECD is

• Organisation

  for Economic Co-operation and Development

• Orientation

  for Economic Co-operation and Development

• Organisation

  for Economic Co-operative and Development

• Organisation

  for Economic Co-operation and Discussion

The OECD (Organisation

for Economic Co-operation and Development) Principles of Good Laboratory Practice were

first created by an Expert Group on GLP set up in

• 1977

• 1978

• 1979

• 1980

The principles of GLP are

• Test facility management

• Quality assurance programme

• Equipment

• Receipt, handling, sampling and storage

General Requirements for GLP consists of

• Appropriately qualified personnel

• Adequate resources

• Appropriate procedures for: sanitation, health precautions, clothing, test

  protocol development, test methods, data analysis, report development, appropriately

  qualified study director, quality assurance function.

“The Study Director” has overall responsibility for the technical conduct of the study,

as well as for the interpretation, analysis, documentation, and reporting of results, and

represents the single point of study control.” This was done by the act OECD in the year of

• 1968

• 1978

• 1988

• 1998

The full form of GLP is

• Good Lab Practice

• Good Leader Practice

• Good Laboratory Practices

• Good Lab Promotion

GLP describes

good practices for non-clinical lab studies that support research or marketing approvals for

• FDA regulated products

• FDA controlled products

• FDA products

• FDA related products

Properties of biological test systems are generally

• less complex than physical test system

• More complex than chemical test system

• Mutable than the

  ones of physical/chemical test systems.

• More complex and mutable than the ones of physical/chemical test systems.

The Environmental Health and Safety Division publishes free-off charge documents in

• 6 series

• 5 series

• 7 series

• 8 series