UK Statutory Instrument SI 1999/3106 United Kingdom

The Good Laboratory Practice Regulations 1999

Read it on legislation.gov.uk (opens in a new tab)
Status
In Force
Penalty ceiling
Regulated

Does it bind you?

Business-side roles with duties under this instrument.

Director or Officer1

Other Acts binding the same actors

If a role above is yours, these are the other instruments that most often bind it.

Director or Officer — also bound by 429 other Acts
Companies Act 2006 126 duties

What it requires

Regulations creating concrete business duties or carrying penalties, grouped as the instrument is structured. Titles link to the source text — blue means you’re leaving for legislation.gov.uk.

sch. 1 para. 3 sch. 1 para. 3 Regulated
  • Document and acknowledge SOP deviations in regulatory studiesDirector or Officer
22 other provisions — procedural and definitional
sch. 1 para. 1 Facility management’s responsibilities
sch. 1 para. 2 Study director’s responsibilities
sch. 2 para. 1 Pre-inspection
s.001 Citation and commencement
s.002 Interpretation
s.003 The Good Laboratory Practice Monitoring Authority
s.003 Principal investigator’s responsibilities (opens in a new tab)
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 (opens in a new tab)
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
Schedules

Schedules

0 of 10 shown
10 other schedules
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

Duty extraction and severity labels are Guvnor’s analysis of the instrument, not the instrument itself. Always verify against the linked source text.