1. BASIC TEST FOR DRUGS
[PHARMACEUTICAL SUBSTANCES,
MEDICINAL PLANTS MATERIALS AND DOSAGE FORMS]
2. WHO GUIDELINES FOR QUALITY CONTROL OF HERBAL DRUGS
3. EVALUATION OF COMMERCIAL CRUDE
DRUG FOR INDENTED USE
4. QUALITY ASSURANCE IN
HERBAL DRUG INDUSTRY
5. WHO GUIDELINES ON CURRENT GOOD
MANUFACTURING PRACTICES (cGMP) FOR HERBAL MEDICINES
6. WHO GUIDELINES ON GOOD
AGRICULTURAL AND COLLECTION PRACTICES (GACP) FOR MEDICINAL
PLANTS
7. EU AND ICH GUIDELINES FOR QUALITY CONTROL OF HERBAL DRUGS
8. RESEARCH GUIDELINE FOR
EVALUATING THE SAFETY AND
EFFICACY OF HERBAL MEDICINE
9. STABILITY TESTING OF HERBAL MEDICINES
10. APPLICATION OF VARIOUS
CHROMATOGRAPHIC TECHNIQUES
IN STANDARDIZATION OF HERBAL PRODUCTS
11. PREPARATION OF DOCUMENTS FOR
NEW DRUG APPLICATION AND EXPORT REGISTRATION
12. GMP REQUIREMENTS AND DRUGS AND COSMETICS ACT PROVISIONS
13. GLOBAL REGULATORY REQUIREMENTS
FOR HERBAL MEDICINES
14. WHO GUIDELINES ON SAFETY
MONITORING OF HERBAL MEDICINES
IN PHARMACOVIGILANCE SYSTEMS
15. COMPARISON OF VARIOUS HERBAL
PHARMACOPOEIAS
16. ROLE OF CHEMICAL AND BIOLOGICAL
MARKERS IN STANDARDIZATION OF
HERBAL PRODUCTS