Regulatory library
Regulations in ValDoc's library
ValDoc's library holds 286 provisions from 130 documents across the United States, the European Union and international sources. Each page says in plain words what a regulation asks of lab equipment and which equipment it reaches.
This page is guidance in our words. The regulation's own text governs.
Last updated
United States
- 21 CFR Part 41 provision
- 21 CFR Part 115 provisions
- 21 CFR Part 581 provision
- 21 CFR Part 2071 provision
- 21 CFR Part 2101 provision
- 21 CFR Part 21152 provisions
- 21 CFR Part 2121 provision
- 21 CFR Part 2131 provision
- 21 CFR Part 3141 provision
- 21 CFR Part 6002 provisions
- 21 CFR Part 6011 provision
- 21 CFR Part 6061 provision
- 21 CFR Part 6101 provision
- 21 CFR Part 8203 provisions
- 21 CFR Part 12713 provisions
- 29 CFR Part 19102 provisions
- CDC/NIH Biosafety in Microbiological and Biomedical Laboratories1 provision
- Drug Supply Chain Security Act1 provision
- FDA guidance: Contract Manufacturing Arrangements for Drugs: Quality Agreements1 provision
- FDA guidance: Data Integrity and Compliance With Drug CGMP: Questions and Answers1 provision
- FDA guidance: Part 11, Electronic Records; Electronic Signatures — Scope and Application1 provision
- FDA guidance: Process Validation: General Principles and Practices1 provision
- FDA guidance: Sterile Drug Products Produced by Aseptic Processing1 provision
European Union
- ATEX Directive 2014/34/EU1 provision
- Directive 2000/54/EC1 provision
- EMA GMP questions and answers: nonsterile manufacture1 provision
- EMA Guideline on process validation for finished products1 provision
- EU GDP Guidelines 2013/C 343/017 provisions
- EudraLex Volume 44 provisions
- EudraLex Volume 4, Annex 19 provisions
- EudraLex Volume 4, Annex 22 provisions
- EudraLex Volume 4, Annex 117 provisions
- EudraLex Volume 4, Annex 131 provision
- EudraLex Volume 4, Annex 159 provisions
- EudraLex Volume 4, Annex 161 provision
- EudraLex Volume 4, Annex 171 provision
- EudraLex Volume 4, Annex 193 provisions
- EudraLex Volume 4, Annex 212 provisions
- EudraLex Volume 4, Chapter 12 provisions
- EudraLex Volume 4, Chapter 21 provision
- EudraLex Volume 4, Chapter 36 provisions
- EudraLex Volume 4, Chapter 45 provisions
- EudraLex Volume 4, Chapter 52 provisions
- EudraLex Volume 4, Chapter 63 provisions
- EudraLex Volume 4, Chapter 71 provision
- EudraLex Volume 4, Chapter 81 provision
- EudraLex Volume 4, Chapter 91 provision
- EudraLex Volume 4, Part II4 provisions
- EudraLex Volume 4, Part IV1 provision
- Machinery Directive 2006/42/EC1 provision
- Machinery Regulation (EU) 2023/12301 provision
- Pressure Equipment Directive 2014/68/EU1 provision
International
- ICH Q1A(R2)1 provision
- ICH Q1B1 provision
- ICH Q71 provision
- ICH Q8(R2)1 provision
- ICH Q9(R1)1 provision
- ICH Q101 provision
- ICH Q121 provision
- PIC/S PE 0091 provision
- PIC/S PE 0111 provision
- PIC/S PI 0061 provision
- PIC/S PI 0091 provision
- PIC/S PI 0411 provision
- WHO Technical Report Series 9611 provision
- WHO Technical Report Series 9861 provision
- WHO Technical Report Series 9921 provision
- WHO Technical Report Series 10192 provisions
- WHO Technical Report Series 10332 provisions
- WHO Technical Report Series 10441 provision
Standards
- ISO 13485
- AATB Standards for Tissue Banking
- United States Pharmacopeia
- ISO 9001
- ISO 11135
- ISO 11137
- ISO 11138
- ISO 11140
- ISO 11607
- ISO 12100
- ISO 13408
- ISO 14644
- ISO 14698Withdrawn
- ISO 14971
- ISO 15223
- ISO/IEC 15415
- ISO/IEC 15416
- ISO/IEC 17025
- ISO 17665
- ISO 20387
- ISO 20857
- ISO 21358
- ISO 21360
- ISO 21501
- ISO 21973
- ISO 23412
- ISO 27893
- ISO 6177
- ISPE GAMP 5
- ISPE Baseline Guides
- ISPE Good Practice Guides
- PDA Technical Reports
- IEST Recommended Practices
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