Introduction: This comparative MCQ set focuses on the British Herbal Pharmacopoeia (BHP) and its relationship to other pharmacopoeial standards, particularly the British Pharmacopoeia (BP). Aimed at M.Pharm students studying Herbal and Cosmetic Analysis (MPA 204T), the questions emphasize monograph structure, identification and assay methods, quality control parameters, standardization approaches, botanical nomenclature, extraction and marker compound considerations, and regulatory implications. These MCQs are designed to deepen conceptual understanding, test applied knowledge in analytical techniques, and prepare students for practical and exam scenarios involving herbal drug evaluation and comparative pharmacopoeial interpretation.
Q1. Which statement best describes the primary focus of the British Herbal Pharmacopoeia (BHP) compared to the British Pharmacopoeia (BP)?
- Comprehensive monographs for synthetic pharmaceuticals with emphasis on formulations
- Monographs for medicinal plants including traditional uses and herbal preparations
- Regulatory guidelines for clinical trials of herbal products only
- General pharmacology texts for education purposes
Correct Answer: Monographs for medicinal plants including traditional uses and herbal preparations
Q2. Which element is more emphasized in a BHP monograph than in a typical BP monograph?
- Assay of a single pure synthetic active ingredient
- Botanical identification, including macroscopic and microscopic features
- Sterility testing for injectable products
- In vivo pharmacokinetic data
Correct Answer: Botanical identification, including macroscopic and microscopic features
Q3. In a comparative context, which type of test is commonly unique to herbal pharmacopoeial standards like BHP?
- Loss on drying
- Foreign matter and botanical purity assessment
- pH of aqueous solution
- Heavy metal limits expressed only as mg/kg
Correct Answer: Foreign matter and botanical purity assessment
Q4. Which analytical technique is often recommended by the BHP for fingerprinting complex herbal extracts?
- Potentiometric titration
- High-performance thin-layer chromatography (HPTLC) or HPLC fingerprinting
- Simple UV spectrophotometry at single wavelength
- Paper chromatography for quantitative assay
Correct Answer: High-performance thin-layer chromatography (HPTLC) or HPLC fingerprinting
Q5. How does BHP typically express assay requirements for herbal drugs compared with BP assay approaches?
- Only absolute purity and weight percentage of all constituents
- Quantification of marker compounds or marker ranges rather than a single defined API potency
- No quantitative requirements, only organoleptic descriptions
- Only biological assays are accepted
Correct Answer: Quantification of marker compounds or marker ranges rather than a single defined API potency
Q6. Which of the following is a common feature of BHP monographs regarding plant part specification?
- Plant part is not specified; whole plant is assumed
- Explicit specification of the plant part used (e.g., leaf, root, rhizome) and its state (dried, fresh, powdered)
- Only the genus is mentioned; species and part omitted
- Only traditional preparation method described without plant part
Correct Answer: Explicit specification of the plant part used (e.g., leaf, root, rhizome) and its state (dried, fresh, powdered)
Q7. When comparing contaminants testing between BHP and BP, which statement is correct?
- BHP ignores pesticide residues while BP mandates them
- BHP includes specific guidance on common herb-related contaminants (pesticides, aflatoxins, microbial limits) tailored to herbal materials
- BP covers microbial limits only for herbal products
- BHP requires radiochemical testing for all herbs
Correct Answer: BHP includes specific guidance on common herb-related contaminants (pesticides, aflatoxins, microbial limits) tailored to herbal materials
Q8. Which of the following best describes the role of pharmacognostic tests in BHP monographs?
- They are optional and not recommended
- They provide morphological and anatomical criteria to ensure correct botanical identity and detect adulteration
- They are replaced by pharmacokinetic profiling
- They only apply to finished herbal formulations, not raw materials
Correct Answer: They provide morphological and anatomical criteria to ensure correct botanical identity and detect adulteration
Q9. In BHP, the term “marker compound” most accurately refers to which concept?
- The toxic impurity in an herb
- A constituent used for identification and/or quantification that serves as an indicator of quality
- The solvent used for extraction
- A synthetic standard unrelated to the plant
Correct Answer: A constituent used for identification and/or quantification that serves as an indicator of quality
Q10. For standardization of extracts, BHP frequently recommends which approach?
- Standardization solely based on dry residue weight
- Standardization to one or more marker compounds and an overall chromatographic fingerprint
- No standardization, relying on traditional use only
- Standardization exclusively by biological potency assays
Correct Answer: Standardization to one or more marker compounds and an overall chromatographic fingerprint
Q11. Which aspect of nomenclature is emphasized in BHP monographs for clarity and global use?
- Use of only common local names
- Use of accepted botanical Latin binomial with author citation and, where relevant, synonyms
- Use of chemical names for active constituents only
- Use of proprietary brand names
Correct Answer: Use of accepted botanical Latin binomial with author citation and, where relevant, synonyms
Q12. How does BHP approach descriptions of traditional use and indications compared with BP?
- BHP typically includes concise notes on traditional uses and customary preparations, whereas BP focuses on pharmacological indications for licensed drugs
- BHP provides no information on traditional use
- BP includes traditional herbal formulations extensively while BHP omits them
- Both BHP and BP ignore traditional information and list only clinical trial data
Correct Answer: BHP typically includes concise notes on traditional uses and customary preparations, whereas BP focuses on pharmacological indications for licensed drugs
Q13. When confronting adulteration, which test strategy is recommended in BHP monographs?
- Only color comparison with an image
- Combined use of macroscopic/microscopic examination, chromatographic fingerprinting and targeted assays for suspected adulterants
- Sole reliance on organoleptic (taste and smell) tests
- Disqualify all samples from non-certified sources without testing
Correct Answer: Combined use of macroscopic/microscopic examination, chromatographic fingerprinting and targeted assays for suspected adulterants
Q14. Which statement reflects BHP’s guidance on extraction solvents for monograph assays?
- Any solvent may be used without specification
- BHP specifies extraction solvents and procedures appropriate for the constituent class to ensure reproducible assays
- BHP mandates water extraction for all herbs
- BHP prohibits organic solvents for any assay
Correct Answer: BHP specifies extraction solvents and procedures appropriate for the constituent class to ensure reproducible assays
Q15. In comparative evaluation, how are reference standards handled in BHP?
- BHP does not use reference standards
- BHP provides or references authenticated reference materials and chromatographic reference standards for key markers
- BHP requires only in-house unlabeled references
- BHP accepts any commercial material without authentication
Correct Answer: BHP provides or references authenticated reference materials and chromatographic reference standards for key markers
Q16. Which of the following is primarily a quality attribute defined in many BHP monographs?
- Clinical trial endpoints
- Loss on drying, extractive values, ash values and purity tests specific to the herbal material
- Prescription-only status
- Cost-effectiveness metrics
Correct Answer: Loss on drying, extractive values, ash values and purity tests specific to the herbal material
Q17. Which regulatory implication is true when a herb appears both in BHP and BP?
- BHP entries automatically supersede BP legal status
- BP monographs may be used for quality requirements of herbal preparations that are recognized medicinal products, while BHP provides complementary botanical and traditional information
- Only BHP can be used for any regulatory submissions
- BP and BHP are identical in content and scope
Correct Answer: BP monographs may be used for quality requirements of herbal preparations that are recognized medicinal products, while BHP provides complementary botanical and traditional information
Q18. For chemical assays in BHP, which validation parameter is emphasized due to complex matrices?
- No validation is required for herbal assays
- Robustness and specificity to distinguish markers from matrix interferences
- Only linearity is important
- Validation only for synthetic APIs is necessary
Correct Answer: Robustness and specificity to distinguish markers from matrix interferences
Q19. In a comparative study, which aspect of stability testing is given special attention for herbal materials in BHP?
- Only thermal degradation of pure APIs
- Stability of marker compounds, influence of storage on organoleptic properties, and susceptibility to microbial growth
- Only photostability is considered
- Stability testing is identical for all herbal and synthetic products with no differences
Correct Answer: Stability of marker compounds, influence of storage on organoleptic properties, and susceptibility to microbial growth
Q20. Which practice is encouraged by BHP to ensure traceability and reproducible quality of herbal raw materials?
- Use of anonymous bulk purchases without documentation
- Documentation of botanical provenance, cultivation/collection data, and batch-linked analytical records
- Reliance solely on supplier verbal assurance
- Exclusion of botanical authentication if chromatographic results are acceptable
Correct Answer: Documentation of botanical provenance, cultivation/collection data, and batch-linked analytical records

I am a Registered Pharmacist under the Pharmacy Act, 1948, and the founder of PharmacyFreak.com. I hold a Bachelor of Pharmacy degree from Rungta College of Pharmaceutical Science and Research. With a strong academic foundation and practical knowledge, I am committed to providing accurate, easy-to-understand content to support pharmacy students and professionals. My aim is to make complex pharmaceutical concepts accessible and useful for real-world application.
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