Quality Management System
Design, implementation and improvement of a robust, risk-based QMS.
- Deviation, CAPA & change control
- Quality risk management (ICH Q9)
- Internal & supplier audits
Pharmaceutical Consulting · Dhaka
Compliance-ready pharma operations, guided by veterans.
Pharmacube Bangladesh helps pharmaceutical manufacturers solve real problems in Production, Quality Assurance, Engineering and Regulatory Affairs — from GMP gap analysis and validation to dossier review and audit readiness.
2020Serving since
11–50Industry professionals
9+Specialised service areas
End-to-end support
From gap to compliance
One partner for every stage of your quality journey.
✓
GMP Gap AssessmentIdentify risks before the inspector does
✓
Qualification & ValidationDQ, IQ, OQ, PQ, process & cleaning validation
✓
Documentation & QMSSOPs, BMRs, CAPA, change control, deviations
✓
Regulatory & Dossier SupportCTD dossier review and submission readiness
Our work is aligned with
- WHO‑GMP
- PIC/S
- ICH Guidelines
- EU‑GMP
- US FDA cGMP
- DGDA
Experience you can rely on.
Founded in 2020 by seasoned pharmaceutical professionals, Pharmacube brings decades of shop-floor and regulatory experience to every engagement.
Our MissionProvide efficient and innovative solutions to our clients' regulatory and operational challenges.
Our VisionTo be Bangladesh's most trusted partner for pharmaceutical quality and compliance.
About Pharmacube
A consulting firm built by people who've run pharma plants.
Pharmacube Bangladesh is a Dhaka-based consulting partnership run by veteran professionals from the pharmaceutical industry. We provide technical advice and hands-on services for operation monitoring and documentation across Production, Quality Assurance and Engineering.
Whether you are preparing for a regulatory inspection, commissioning a new facility, registering a product for export, or strengthening your quality culture, our team works alongside yours to deliver practical, inspection-ready results.
- Veteran-led team
- Practical, on-site support
- Local regulatory insight
- International standards
What We Do
Comprehensive services for the pharmaceutical sector
Flexible support — from a single validation project to a full plant compliance programme.
Plant Accreditation & Certification
End-to-end preparation for national and international GMP inspections.
- GMP gap analysis & remediation
- Mock inspections
- WHO, PIC/S & export-market readiness
Qualification, Calibration & Validation
Documented evidence that your facility, equipment and processes perform as intended.
- DQ, IQ, OQ, PQ protocols & reports
- Process, cleaning & analytical validation
- HVAC, water & utilities qualification
R&D and Dossier Review
Technical review that strengthens product development and registration files.
- CTD / eCTD dossier review
- Formulation & stability data review
- Technology transfer support
Documentation Support
Clear, compliant documents that your team can actually follow.
- SOPs, BMRs & BPRs
- Site Master File & VMP
- Data integrity (ALCOA+) practices
GMP & Pharmacovigilance Training
Practical training programmes that build a lasting quality culture.
- cGMP & GDP for all levels
- Pharmacovigilance systems
- On-site workshops & assessments
Regulatory & Compliance Services
Guidance through local and international regulatory requirements.
- DGDA submissions & liaison
- Export registration support
- Compliance audits & remediation
Production, QA & Engineering Monitoring
Operational oversight that keeps your plant efficient and in control.
- Operation monitoring & batch review
- Maintenance & engineering systems
- Productivity & yield improvement
Raw Material Supply
Sourcing support for quality APIs, excipients and packaging materials.
- Qualified supplier sourcing
- Vendor qualification support
- Documentation & CoA review
Our Approach
A clear path from challenge to compliance
Every engagement follows a structured, transparent process so you always know where things stand.
Assess
On-site review of facilities, systems and documents to identify gaps, risks and priorities.
Plan
A practical roadmap with clear deliverables, timelines and responsibilities agreed with your team.
Implement
Hands-on execution — protocols, documentation, validation and training delivered alongside your staff.
Sustain
Follow-up audits and continuous improvement so you stay inspection-ready, not just once.
Why Pharmacube
Why manufacturers choose to work with us
We combine deep industry experience with a practical, results-focused approach.
01
Veteran Expertise
Our consultants have held senior roles in production, QA and engineering at pharmaceutical plants.
02
Practical Solutions
Advice that works on the shop floor — not just on paper.
03
Local + Global Knowledge
Deep understanding of DGDA requirements and international GMP expectations.
04
One-Stop Partner
From documentation to validation to training — one team, fully coordinated.
05
Confidential & Ethical
Your data, processes and products are handled with complete confidentiality.
06
Cost-Effective
Flexible engagements sized to your needs — project-based or ongoing retainer.
Who We Serve
Supporting every corner of the pharma industry
Finished Dosage ManufacturersSolids, liquids, semi-solids and sterile products
API & Excipient ProducersActive ingredient and raw material facilities
Herbal, Unani & AyurvedicTraditional medicine manufacturers
Veterinary PharmaceuticalsAnimal health product manufacturers
New Plant ProjectsGreenfield & expansion projects from design stage
Export-Oriented CompaniesBusinesses targeting regulated international markets
FAQ
Frequently asked questions
What kind of companies does Pharmacube work with?
We work with pharmaceutical manufacturers of all sizes — from established plants preparing for international inspections to new facilities being set up from the ground up — as well as API, herbal and veterinary producers.
Can you help us prepare for a GMP inspection?
Yes. We conduct a detailed gap assessment, help close the gaps through documentation, validation and training, and run mock inspections so your team is confident on inspection day.
Do you provide on-site services?
Yes. Most of our qualification, validation, monitoring and training work is carried out on-site at the client's facility, working directly with your team.
How are engagements structured?
We offer project-based engagements for defined scopes (such as a validation project or dossier review) and ongoing retainer support for continuous QA and compliance needs.
How do we get started?
Simply send us a message or call us. We'll schedule an initial discussion to understand your needs and then propose a scope, timeline and quotation.
Facing a regulatory or quality challenge?
Talk to our experts — we'll help you find the most efficient way forward.
Contact Us
Let's discuss your project
Reach out for a consultation, a quotation, or just to ask a question. We usually respond within one business day.
OfficeSuite 8/B, Pragati Sarani, Dhaka 1229, Bangladesh
Get directions →
Get directions →
Phone+880 1XXX-XXXXXX
Office HoursSaturday – Thursday, 9:00 AM – 6:00 PM