The Good Laboratory Practice Regulations 1999

s.sch001

Waste Disposal

s.sch002

Standard operating procedures

s.sch002

Performance of the study

s.sch002

Reporting of study results

s.sch002

Storage and retention of records

s.sch002

Facilities

s.sch002

Care, housing and containment of biological test systems

s.sch002

Apparatus, materials, reagents and specimens

s.sch002

Test systems

s.sch002

Test and reference items

sch. 1 para. 1

Facility management’s responsibilities

sch. 1 para. 2

Study director’s responsibilities

sch. 1 para. 3

sch. 1 para. 3

sch. 2 para. 1

Pre-inspection

s.001

Citation and commencement

s.001

Facility management’s responsibilities

s.002

Interpretation

s.002

Study director’s responsibilities

s.003

The Good Laboratory Practice Monitoring Authority

s.003

Principal investigator’s responsibilities

s.004

Requirement to be a member or a prospective member of the United Kingdom good laboratory practice compliance programme

s.004

Study personnel’s responsibilities

s.005

Prospective membership of the United Kingdom good laboratory practice compliance programme

s.006

Membership of the United Kingdom good laboratory practice compliance programme

s.007

Requirement to adhere to the principles of good laboratory practice

s.008

Appeals against warning notices

s.009

Powers of entry etc.

s.010

Disclosure of confidential information

s.011

Obstruction etc. of authorised persons

s.012

False good laboratory practice instruments

s.013

Offences by bodies corporate and Scottish partnerships

s.014

Defence of due diligence

s.015

Penalties

s.016

Fees

s.017

Revocation