Quascenta
Quascenta, operating as PQMS, builds a cloud-based SaaS suite of five modules for pharmaceutical and biotech validation, quality management, cleaning validation and electronic logbooks, sold via modular subscriptions to manufacturers in regulated industries.
- Company typePrivate
- Founded2001
- HeadquartersSingapore, Singapore
- Headcount11–50
- GTM typeB2B
- OfferingSoftware
What Quascenta does
Quascenta Pte. Ltd., operating under the brand PQMS, is a Singapore-headquartered software company that has been building pharmaceutical validation and process management software since 2001. The company sells the PQMS Software Suite, a cloud-based, multi-tenant SaaS platform on AWS serving pharmaceutical, biotech, food and cosmetic manufacturers. The suite comprises five integrated modules: QMS Pro for quality management including non-conformances, CAPAs and change control; ValDoc Pro for qualification and document management with SOP versioning from MS Word; eProcess Pro for process validation lifecycle tracking and APQR generation; eResidue Pro for cleaning validation and MACO calculations covering formulation, API and biotech; and eLog Pro for electronic GMP logbooks. The architecture is built to GAMP5 Category 4 standards and complies with FDA 21 CFR Part 11, EU GMP Annex 11 and HIPAA, with AWS S3 document storage supporting a claimed 99.99% availability.
Quascenta generates revenue through modular annual SaaS subscriptions that customers can start with individually and expand over time, supplemented by professional services for implementation, qualification and data upload, with delivery led by in-house Subject Matter Experts. GTM is a hybrid model: a self-serve SaaS funnel via pqms.com with a "Book a Demo" CTA, layered with an enterprise field sales motion where SMEs guide prospects and customers through setup, validation and best-practice adoption. The company reports 100+ customers globally (with eResidue Pro alone at that scale since 2004) and operates websites in English, Korean and Japanese, indicating deliberate outreach into Northeast Asian regulated markets.
The firm is privately held with no disclosed institutional funding, no parent company, and approximately 22 employees. There are no announced acquisitions, partnerships or leadership changes in the available material, and the primary moat is regulatory credibility (FDA/EMA/MHRA/ANVISA inspection track record) combined with long-tenured customer relationships in a niche where switching cost is high due to revalidation burden.
Quascenta firmographics
Firmographics- Name
- Quascenta
- Legal name
- Quascenta Pte. Ltd.
- Website
- https://pqms.com
- Company type
- Private
- Founded year
- 2001
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Quascenta, operating as PQMS, builds a cloud-based SaaS suite of five modules for pharmaceutical and biotech validation, quality management, cleaning validation and electronic logbooks, sold via modular subscriptions to manufacturers in regulated industries.
- Ownership category
- akta.pro rank
Quascenta industry classification
Industry- Product category
- Pharmaceutical Validation Software
- NAICS
- Software Publishers (51321)
- SIC
- Services-Prepackaged Software (7372)
- akta.pro primary industry
- Quality, Compliance & Validation Software for Labs (GxP/CSV, eQMS for QC Labs) (HLAGAJAI)
- akta.pro secondary industry
- Food Quality Management System (QMS) Design & Implementation (AFALALAA)
Keywords
Where Quascenta is headquartered
LocationHeadquarters
- HQ city
- Singapore
- HQ country
- Singapore
- HQ region
- Asia
Offices1 record
Markets served
Quascenta business model
Business model- GTM type
- B2B
- Offering type
- Software
- Cost components
- Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
Revenue model
- Software Subscriptions (SaaS): Modular subscription model where customers can subscribe to individual modules (QMS Pro, ValDoc Pro, eProcess Pro, eResidue Pro, eLog Pro) based on current requirements and upgrade as needs evolve. Cloud-hosted delivery eliminates site-based installations.
- Professional Services: Implementation services, qualification support, and data upload services. In-house SMEs provide consultancy support including reviewing current practices and recommending changes in line with best practices. Expert guidance covers setting up compliant and audit-ready programs.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Subscription | Annual | Modular subscription with per-module pricing |
Go-to-market motion2 records
Distribution channels2 records
Marketing channels3 records
Quascenta product offering
Product offeringCore offering
Quascenta develops and sells the PQMS Software Suite, a modular cloud-based SaaS platform designed by SMEs for SMEs in the pharmaceutical, biotech, food, and cosmetic industries. The suite comprises five integrated modules covering quality management (QMS Pro), qualification and document management (ValDoc Pro), process validation (eProcess Pro), cleaning validation with MACO calculations (eResidue Pro), and digital GMP logbooks (eLog Pro). The platform replaces paper-based validation workflows with electronic, audit-ready, regulatory-compliant processes under 21 CFR Part 11, EU GMP Annex 11, and HIPAA.
Product overview
PQMS (Process Quality Management Suite) is a modular software platform designed by Quascenta for pharmaceutical, biotech, food, and cosmetic industries. The suite consists of five integrated modules: QMS Pro (quality management system for non-conformances, CAPAs, and change control), ValDoc Pro (qualification and document management), eProcess Pro (process validation and CPV monitoring), eResidue Pro (cleaning validation and MACO calculations), and eLog Pro (digital GMP logbook). These modules work together seamlessly to cover the full spectrum of quality and compliance needs from commissioning and qualification through process management to cleaning validation.
Differentiator
Problem solved
Functional benefit
Brands
- QMS Pro: Comprehensive quality management system for managing non-conformances, CAPAs, and change control with embedded root cause analysis and risk analysis tools.
- ValDoc Pro
- eProcess Pro
- eResidue Pro
- eLog Pro
Products and services
- PQMS Software Suite A comprehensive, modular software platform consisting of five integrated modules covering the full spectrum of quality and compliance needs for pharmaceutical, biotech, food, and cosmetic industries. Customers can subscribe to individual modules and expand as requirements evolve.
- QMS Pro
Quantifiable outcome
- eResidue Pro has been in use since 2004 with 100+ customers globally
- +3 more outcomes
Companies that use Quascenta
Customer profileNamed customers1 record
Segments4 records
Ideal customer profiles4 records
Quascenta technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Integration7 records
Feature7 records
Quascenta partnerships and signals
Strategic signalScale indicators3 records
Recent moves5 records
Expansion highlights5 records
Quascenta competitors and assessment
Company assessmentDirect peers
- Veeva Systems: Veeva's Vault Quality, Vault Validation, and related applications provide cloud QMS and validation management for life sciences, directly competing with Quascenta's PQMS suite for pharma quality and compliance budgets.
- Kneat Solutions: Kneat's validation lifecycle management software targets the same regulated computer-system and equipment validation use cases as ValDoc Pro and eProcess Pro in pharma and biotech.
- MasterControl: MasterControl offers a GxP-compliant QMS platform purpose-built for life sciences manufacturers, overlapping directly with QMS Pro, ValDoc Pro, and eProcess Pro across validation and quality workflows.
- Greenlight Guru: Greenlight Guru provides purpose-built quality management software for medical device and life sciences companies, addressing similar validation, CAPA, and electronic quality system needs as PQMS modules.
- Sparta Systems (TrackWise, Honeywell): TrackWise is an enterprise QMS widely used across pharma and biotech for non-conformance, CAPA, change control, and audit management - directly overlapping with QMS Pro functionality.
- Dot Compliance: Dot Compliance delivers a cloud eQMS built on Salesforce for pharma and medical device manufacturers, competing head-on with Quascenta for mid-market regulated QMS and CAPA workflows.
Emerging players
- ComplianceQuest: ComplianceQuest offers a next-generation, Salesforce-based QMS for life sciences and manufacturing, targeting the same regulated mid-market buyers as Quascenta with comparable quality and compliance modules.
- AssurX: AssurX provides regulated-industry quality and compliance management software with strength in life sciences, competing for similar CAPA, change control, and document control workloads as PQMS.
Broad incumbents
- BIOVIA (Dassault Systèmes): BIOVIA provides quality, validation, and process management solutions for life sciences and manufacturing, overlapping with Quascenta's process validation, QMS, and cleaning validation offerings.
- ETQ (Hexagon): ETQ Reliance is a broad enterprise QMS platform used in regulated industries including life sciences, offering overlapping quality, document, and compliance capabilities at a larger scale than Quascenta.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks7 records
Key highlights7 records
Customer concentration
Quascenta social profiles
Digital presenceQuascenta compliance and trust
Trust signalCompliance4 records
Quascenta financial estimates
Financial estimateRevenue estimate
Valuation estimate
Quascenta leadership team
Management profileNumber of profiles
Profiles1 record
Quascenta funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Quascenta M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Quascenta
What does Quascenta do?
Quascenta develops and sells the PQMS Software Suite, a modular cloud-based SaaS platform designed by SMEs for SMEs in the pharmaceutical, biotech, food, and cosmetic industries. The suite comprises five integrated modules covering quality management (QMS Pro), qualification and document management (ValDoc Pro), process validation (eProcess Pro), cleaning validation with MACO calculations (eResidue Pro), and digital GMP logbooks (eLog Pro). The platform replaces paper-based validation workflows with electronic, audit-ready, regulatory-compliant processes under 21 CFR Part 11, EU GMP Annex 11, and HIPAA.
Is Quascenta a public or private company?
Quascenta is a private company. It is classified as founder individual operated bootstrapped and is currently operating.
When was Quascenta founded?
Quascenta was founded in 2001. It employs 11 to 50 people.
Where is Quascenta based?
Quascenta is headquartered in Singapore, Singapore, in the Asia region.
How does Quascenta make money?
Two revenue lines are on record. Software Subscriptions (SaaS) is the primary driver. The others are professional Services.
Who are Quascenta's main competitors?
Direct peers on record are Veeva Systems, Kneat Solutions, MasterControl, Greenlight Guru, Sparta Systems (TrackWise, Honeywell) and Dot Compliance. Emerging players are ComplianceQuest and AssurX. Broad incumbents are BIOVIA (Dassault Systèmes) and ETQ (Hexagon).
Does Quascenta have an API?
No public API is recorded for Quascenta.
What industry is Quascenta in?
Quascenta's product category is Pharmaceutical Validation Software. Its primary akta.pro industry code is HLAGAJAI, Quality, Compliance & Validation Software for Labs (GxP/CSV, eQMS for QC Labs), with a secondary code of AFALALAA, Food Quality Management System (QMS) Design & Implementation. Its NAICS code is 51321 and its SIC code is 7372.