Research & Development (R&D)
- Excipient selection by functional category and typical concentration
- Starting formulations and batch formulae for eight dosage forms
- HLB, isotonicity and Henderson–Hasselbalch buffer calculations
Pharmaceutical Knowledge Hubمرکز دانش دارویی
Integrated knowledge, sharper decisions, smarter drug development
For professionals in research and development (R&D), procurement and supply chain, quality control (QC), quality assurance (QA) and regulatory affairs (RA); faculty and students of pharmacy and pharmaceutical sciences; everyone working in the pharmaceutical sector; and pharmacies.
Sections
Pharmaceutical Knowledge Hub
Evidence-based
Functional categories, concentration ranges and specifications traceable to compendial and ICH references
Development-oriented
Covers the path from pre-formulation and excipient selection to scale-up and technology transfer
GMP & regulatory-ready
Procedures and references structured around PIC/S GMP, the ICH Q series and the CTD (ICH M4)
The specialist reference for pharmaceutical knowledge, information and tools
From raw material sourcing and formulation development to technical calculations and quality and regulatory requirements — built on authoritative, citable scientific sources.
Find who manufactures or imports a raw material in Iran — APIs, excipients, vitamins, mineral salts, supplement and cosmetic ingredients — with phone, email, website and the source of every record.
Browse by category
Who it is for
Every department of a pharmaceutical company — and students and pharmacists — gets the references and tools they use every day, in one subscription.
Inside the vault
The sections are designed to work together: from an excipient you move to its suppliers, to the calculation that uses it and to the regulatory requirement that governs it.
Iranian manufacturers and importers of APIs, excipients, vitamins, mineral salts, supplement and cosmetic raw materials, with contact details, searchable by material.
139 companies · 2,164 materials
Open sectionDosage-form references for solid, semi-solid, liquid, sterile and biological products, from formulation design to scale-up.
8 titles · 36 chapters
Open sectionFunctional category, typical concentration range, dosage-form applicability and CAS number for each excipient.
272 excipients · 25 functional categories
Open sectionActive pharmaceutical ingredients, vitamins and mineral salts with CAS number, molecular weight and a key physicochemical or stability note.
810 materials · 15 classes
Open sectionFormulation, physical pharmacy and analytical calculations: potency, HLB, powder flow, capsule fill, coating, isotonicity, osmolarity, buffers, stability kinetics, HPLC and UV assay, system suitability, linearity, dissolution and f2, content uniformity, Karl Fischer and titration.
50 calculators
Open sectionStarting compositions by dosage form with the functional role of each component, q.s. balancing and batch quantities.
8 dosage forms
Open sectionCTD module structure, the core ICH quality guidelines and ICH Q1A(R2) stability storage conditions.
6 CTD sections · 20 ICH guidelines
Open sectionPharmacopoeial tests and acceptance criteria, microbial limits for non-sterile products, pharmaceutical water, ICH Q2 method validation and OOS investigation.
27 laboratory SOPs · 11 microbiology SOPs
Open sectionThe pharmaceutical quality system (ICH Q10), quality risk management tools and a GMP-aligned SOP library for every department, with full text.
145 SOPs · 7 departments
Open sectionOrganisation-wide access, role-based permissions, company-specific handbooks and bespoke software.
Open sectionDatabases
Structured records searchable in Persian and English — by INN, salt form, trade name or CAS Registry Number.
Pharmaceutical calculations
From potency, powder flow and capsule fill to buffer capacity, stability kinetics, HPLC assay, system suitability, dissolution f2 and content uniformity. Each calculator states its governing equation and its pharmacopoeial or ICH reference.
m = LC × SF × 100 / [Assay × (100 − W − RS) / 100]
HLB_mix = f_A·HLB_A + f_B·HLB_B
CI = 100·(V₀ − V_f)/V₀ ; HR = V₀/V_f
W_agent = (0.009·V − Σ m_drug·E) / E_agent
pH = pKa + log([A⁻]/[HA])
%LC = (A_u/A_s)·C_s·V_u·(W̄/W_u)/LC × 100
f2 = 50·log{[1 + (1/n)Σ(R_t − T_t)²]^−0.5 × 100}
AV = |M − X̄| + k·s
Getting started
Individual or Team / Organisation — according to the number of users and the sections your work needs.
Create an account with your mobile number and pay online; companies can also ask for a pro-forma invoice.
Your sections open as soon as the payment is confirmed; the end date and renewal are in your account.
Plans
Two ways to subscribe: an individual licence for one user on one IP, or a team licence for six or more users. Prices are in Toman per month.
For specialists and formulators, students and pharmacies
Full access to all 9 sections · 1 user on 1 IP
2,601,00015% off
2,210,000Toman per month
against buying the 9 sections separately
Or a single section: 289,000 Toman per month
For R&D, QC, QA, regulatory and supply teams of pharmaceutical companies
6 users on different IPs · full access
13,260,00010% off
11,934,000Toman per month
against six individual subscriptions
Each additional user from the 7th: 1,000,000 Toman per month
Estimate your monthly cost
Individual
Monthly total
2,601,000 Toman15% off
2,210,000 Toman per month
Team / Organisation
Monthly total
13,260,000 Toman10% off
11,934,000 Toman per month
1,989,000 Toman per user
| Individual | Team / Organisation | |
|---|---|---|
| Users | 1 user on 1 IP | 6 or more, on different IPs |
| Monthly price | 2,210,000 (all 9 sections) | 11,934,000 (6 users) |
| Single-section subscription | 289,000 per section | |
| Additional users | 1,000,000 per user | |
| All 9 specialised sections | ||
| Supplier & manufacturer bank | ||
| Pharmaceutical calculators and formulation tools | ||
| SOP library, QA and QC references | ||
| CTD and ICH regulatory references | ||
| User management by the unit head | ||
| Official quotation for the company | ||
| Dedicated support |
A handbook written around your products, production lines and procedures.
A calculation or formulation tool built on your data and your way of working.
A copy of the databases with restricted access, for use inside the organisation.
Questions
Regulatory sections follow the ICH guidelines (including M4 for the CTD and Q1A(R2) for stability), and the SOPs reference PIC/S GMP and the relevant ICH guidelines. Excipient functions and concentration ranges are working guidance to be confirmed against the current pharmacopoeias and the Handbook of Pharmaceutical Excipients. Every record in the supplier bank shows its source.
No. PharmaVault is a working reference that shortens the search; specifications, limits and registration requirements must always be confirmed against the current official editions and the requirements of the Iran Food and Drug Administration.
Send a request with the button of the plan you need. After the request is confirmed and paid, the sections of your plan are opened for the users you named.
An individual subscription is for one user on one IP. For several people, the Team / Organisation plan starts at six users on different IPs, managed by the head of the unit, and more users can be added.
Yes. Custom handbooks, company-specific software and database licences can be ordered separately from a subscription or together with the Team / Organisation plan.
Email us the company's name, products and a verifiable source such as its website or syndicate listing.
Contact
Request access for yourself, or ask for a Team / Organisation quotation for your department or company.
info@pharmavault.ir