Iran Pharmacy Ph.D. Entrance Exam study plan
Iran Pharmacy Ph.D. Entrance Exam · Give each week a clear focus.
8 weeks · About 7 hours per week
Pharmaceutics and Pharmaceutical Technology (including dosage form design, drug delivery, and biopharmaceutics)
Map the biopharmaceutics classification system onto 20 common Iranian-market drugs and write the solubility/permeability rationale for each
Derive the Noyes-Whitney and Higuchi equations from scratch and solve three numeric release-rate problems without notes
List the mechanisms and formulation levers for each of the four BCS classes and match them to a plausible dosage-form strategy
Build a one-page table of excipient functions (diluent, binder, disintegrant, lubricant, glidant) with two examples and typical concentration ranges
Your checkpoint
A 10-page handwritten summary of biopharmaceutics fundamentals plus 15 solved numeric problems with worked steps
Pharmaceutics and Pharmaceutical Technology (including dosage form design, drug delivery, and biopharmaceutics)
Compare immediate-release, extended-release, and delayed-release kinetics and sketch plasma concentration-time curves for each
Explain the design logic of matrix, reservoir, osmotic, and multiparticulate systems and identify the rate-controlling step in each
Calculate loading dose, maintenance dose, and accumulation factor for a two-compartment scenario given clearance and volume
Evaluate how particle size, polymorphism, and salt form alter dissolution and bioavailability
Your checkpoint
A comparison chart of six modified-release technologies with rate-controlling mechanisms plus 10 solved pharmacokinetic dosing calculations
Pharmacology and Toxicology
Draw dose-response curves for full, partial, and inverse agonists and explain potency versus efficacy with labeled axes
Classify receptor families (GPCR, ion channel, nuclear, enzyme-linked) and match each to two drug examples and their downstream signaling
Explain the mechanisms of competitive, noncompetitive, and irreversible antagonism and predict the effect of increasing antagonist concentration on Emax and EC50
Describe the pathways of drug metabolism (phase I and phase II) and predict how induction or inhibition of CYP3A4 changes plasma levels of a narrow-therapeutic-index drug
Your checkpoint
A one-page receptor and signal-transduction reference sheet plus 20 solved pharmacodynamics problems
Pharmacology and Toxicology
Summarize the mechanism, major adverse effects, and antidote or management for organophosphate, opioid, paracetamol, iron, and methanol poisoning
Explain the toxicokinetic concepts of volume of distribution, half-life, and dialysis eligibility for common overdoses
Describe the pharmacology of autonomic drugs class by class (cholinergic, anticholinergic, adrenergic agonists and blockers) with one clinical use each
Outline the mechanism and monitoring parameters for drugs acting on the cardiovascular and renal systems
Your checkpoint
A toxicology antidote quick-reference card plus a 30-question self-test scored and reviewed with error notes
Medicinal Chemistry and Drug Design & Pharmaceutical Analysis and Instrumental Methods
Draw the physicochemical and stereochemical properties that govern receptor binding and relate them to the pharmacophore concept
Explain structure-activity relationships for at least three drug classes (for example, sulfonamides, beta-lactams, and benzodiazepines) using specific substituent effects
Apply Lipinski's rule of five and bioisosteric replacement to propose modifications to a lead compound
Interpret IR, UV-Vis, 1H-NMR, and mass spectra of simple drug molecules and assign key peaks
Set up and validate a simple HPLC assay: choose column, mobile phase, detection wavelength, and acceptance criteria
Your checkpoint
A worked medicinal-chemistry case study proposing two analogs with justification plus a fully written HPLC method validation protocol
Pharmacognosy and Natural Products Chemistry (phytochemistry and medicinal plant sciences) & Clinical Pharmacy and Pharmacotherapy
Classify secondary metabolites (alkaloids, terpenoids, phenolics, saponins, flavonoids) by biosynthetic origin and give a plant source and activity for each class
Describe extraction, fractionation, and chromatographic isolation workflows and the role of TLC and column chromatography in dereplication
Evaluate the evidence for three medicinal plants used in Iranian traditional medicine and state the pharmacological mechanism claimed
Construct a pharmacotherapy plan for a patient with type 2 diabetes and hypertension, including drug selection, monitoring, and counseling points
Your checkpoint
A phytochemistry metabolite map plus one complete pharmaceutical care plan with monitoring parameters and patient counseling notes
Pharmaceutical Biotechnology and Molecular Biology & General English for Pharmaceutical Sciences
Explain recombinant DNA workflow from gene cloning through expression host selection to protein purification and quality control
Describe the principles of PCR, ELISA, Western blot, and monoclonal antibody production and state one pharmaceutical application of each
Summarize the regulatory and immunogenicity considerations for biosimilars versus originator biologics
Practice reading pharmaceutical scientific abstracts and answer comprehension questions on methods, results, and limitations
Your checkpoint
A glossary of 40 biotechnology terms with definitions plus three abstract-comprehension exercises scored against a rubric
Research Methodology, Biostatistics, and Pharmacy Ethics & Pharmaceutics and Pharmaceutical Technology (including dosage form design, drug delivery, and biopharmaceutics) & Pharmacology and Toxicology
Distinguish study designs (RCT, cohort, case-control, cross-sectional) and select the appropriate statistical test for a given dataset
Calculate and interpret sensitivity, specificity, positive predictive value, confidence intervals, and p-values for a sample dataset
State the core principles of research ethics (informed consent, confidentiality, institutional review, plagiarism, and authorship) and apply them to a short scenario
Complete two timed mixed-domain mock exams and analyze errors by domain
Your checkpoint
A full-length timed mock exam score report with a ranked error log and a written remediation plan for the three weakest domains
Milestones
Week 2: Solve 15 biopharmaceutics and pharmacokinetic numeric problems under timed conditions with at least 80% accuracy and no formula sheet
Week 4: Score at least 75% on a 30-question pharmacology and toxicology self-test and explain every missed item aloud without notes
Week 6: Produce a complete pharmaceutical care plan and a phytochemistry metabolite map that an examiner could grade, with all claims sourced
Week 8: Achieve at least 70% on a full-length timed mock exam covering all nine domains and show a written remediation plan for the three lowest-scoring domains