1 |
PIC S and its role |
Q4B ANNEX 8(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON STERILITY TEST GENERAL CHAPTER |
2 |
PIC S and its role |
Q4B ANNEX 7(R2) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON DISSOLUTION TEST GENERAL CHAPTER |
3 |
PIC S and its role |
Q4B ANNEX 6(R1) Step 2 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON UNIFORMITY OF DOSAGE UNITS GENERAL CHAPTER |
4 |
PIC S and its role |
Q4B ANNEX 5(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON DISINTEGRATION TEST GENERAL CHAPTER |
5 |
PIC S and its role |
Q4B ANNEX 3(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON TEST FOR PARTICULATE CONTAMINATION: SUB-VISIBLE PARTICLES GENERAL CHAPTER |
6 |
PIC S and its role |
Q4B ANNEX 2(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON TEST FOR EXTRACTABLE VOLUME OF PARENTERAL PREPARATIONS GENERAL CHAPTER |
7 |
PIC S and its role |
Q4B ANNEX 1(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON RESIDUE ON IGNITION/SULPHATED ASH GENERAL CHAPTER |
8 |
PIC S and its role |
Q4B ANNEX 4C(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON MICROBIOLOGICAL EXAMINATION OF NON-STERILE PRODUCTS: ACCEPTANCE CRITERIA FOR PHARMACEUTICAL PREPARATIONS AND SUBSTANCES FOR PHARMACEUTICAL USE GENERAL CHAPTER |
9 |
PIC S and its role |
Q4B ANNEX 4B(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON MICROBIOLOGICAL EXAMINATION OF NON-STERILE PRODUCTS: TEST FOR SPECIFIED MICRO-ORGANISMS GENERAL CHAPTER |
10 |
PIC S and its role |
Q4B ANNEX 4A(R1) Step 4 |
EVALUATION AND RECOMMENDATION OF PHARMACOPOEIAL TEXTS FOR USE IN THE ICH REGIONS ON MICROBIOLOGICAL EXAMINATION OF NON-STERILE PRODUCTS:MICROBIAL ENUMERATIONS TESTS GENERAL CHAPTE |
11 |
PIC S and its role |
Q3C(R5) Step 4 |
IMPURITIES: GUIDELINE FOR RESIDUAL SOLVENTS |
12 |
PIC S and its role |
Q3B(R2) Step 4 |
IMPURITIES IN NEW DRUG PRODUCTS |
13 |
PIC S and its role |
Q2(R1) Step 4 |
VALIDATION OF ANALYTICAL PROCEDURES: TEXT AND METHODOLOGY |
14 |
PIC S and its role |
Q1F Step 4 |
STABILITY DATA PACKAGE FOR REGISTRATION APPLICATIONS IN CLIMATIC ZONES III AND IV |
15 |
PIC S and its role |
Q1E Step 4 |
EVALUATION FOR STABILITY DATA |
16 |
PIC S and its role |
Q1D Step 4 |
BRACKETING AND MATRIXING DESIGNS FOR STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS |
17 |
PIC S and its role |
Q1C Step 4 |
STABILITY TESTING FOR NEW DOSAGE FORMS Annex to the ICH Harmonised Tripartite Guideline on Stability Testing for New Drugs and Products |
18 |
PIC S and its role |
Q1B Step 4 |
STABILITY TESTING: PHOTOSTABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS |
19 |
PIC S and its role |
Q1A(R2) Step 4 |
STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS |