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End-to-end consultancy for Medical, AYUSH, Dental, Homoeopathy and Pharmacy institutions — from feasibility and master planning to regulatory applications, inspection readiness, compliance and expansion.
2027 requirements are subject to the regulations, notifications, permissions, standards and application windows applicable at the time of submission.
AR-MAC’S coordinates the institutional, academic, infrastructure, clinical and documentation workstreams around the applicable regulatory ecosystem.
MEDICAL
NMC
Medical education institutional development, MBBS planning, teaching-hospital strategy, assessment readiness and expansion.
AYUSH
NCISM
Ayurveda, Unani, Siddha and Sowa-Rigpa institutional establishment and academic development.
HOMOEOPATHY
NCH
BHMS and applicable postgraduate institutional planning, clinical infrastructure and regulatory readiness.
DENTAL
NDC
National Dental Commission framework for BDS, MDS and dental institutional development. Former DCI terminology may be retained only for historical reference.
PHARMACY
PCI
Pharmacy institutional development covering D.Pharm, B.Pharm, M.Pharm and Pharm.D pathways under the applicable framework.
INSTITUTIONAL
University + State + Local
Regulatory approval is only one layer. Projects may also require state, university, local, safety, environmental and clinical permissions.
A premium institutional-development model designed for promoters, trusts, societies, educational groups and existing institutions.
Know whether the project is viable before committing major capital.
Translate the project vision into a structured institutional roadmap.
Build the evidence base and submission architecture.
Develop the clinical ecosystem around the academic institution.
Align physical learning spaces with programme requirements.
Create the human-resource architecture required for operations and compliance.
Build a traceable equipment and laboratory readiness system.
Prepare the institution to demonstrate what it claims.
Move beyond approval toward sustainable institutional growth.
Every project is organized around measurable gates — feasibility, development, evidence, assessment and continuous compliance.
Promoter vision, programme, location, institution model and growth ambition.
Land, infrastructure, hospital, regulatory and financial feasibility.
Master plan, academic architecture, clinical model and compliance map.
Campus, hospital, laboratories, equipment, HR and academic systems.
Create the regulatory evidence base and institutional document vault.
Application preparation, data verification and submission support.
Mock inspection, physical verification and deficiency prevention.
Approval support, continuing compliance, quality and expansion planning.
AR-MAC’S can structure a live institutional compliance system across regulatory, infrastructure, hospital, faculty, equipment, documents, applications and inspection.
Authority & regulation tracking
Title, site & feasibility
Buildings & facilities
Clinical readiness
HR & qualification
Procurement & compliance
Regulatory evidence
Submission tracking
Assessment preparedness
Ongoing monitoring
A structured readiness review identifies gaps before they become regulatory problems.
Campus & Clinical Audit
Review academic spaces, laboratories, hospital services, equipment, utilities and operational readiness.
Illustrative readiness visualization — not a regulatory score.
Documents & Digital Data
Cross-check institutional records, faculty data, equipment records, clinical statistics and submitted information.
Illustrative readiness visualization — not a regulatory score.
Before major investment, AR-MAC’S can test the project against the fundamentals that determine institutional viability.
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Gate
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Question
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AR-MAC’S review
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A — Authority
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Who regulates the programme?
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Regulatory mapping
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Packages can be customized by regulator, programme, intake, project stage and institutional complexity.
Feasibility & Regulatory
Institution Establishment
Approval & Inspection
Transformation
Yes. A feasibility stage can review the proposed site, programme, regulatory pathway, infrastructure potential and major project risks before substantial investment.
No. Regulatory decisions remain with the competent statutory, government and university authorities. AR-MAC’S provides planning, documentation, compliance and readiness support.
Yes. The framework can be used for compliance audits, inspection preparation, infrastructure strengthening, academic development, programme expansion and institutional transformation.
Yes. A health-sciences project may involve a national regulator, state authorities, university/affiliation authorities and local statutory permissions depending on the programme and project structure.
No. They should be verified against the official notification, regulation or application portal applicable to the relevant academic year and project.
AR-MAC’S provides strategic educational consultancy, regulatory guidance, accreditation support, and institutional development solutions across India
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