Opus Regulatory
Opus Regulatory is a Boston-based regulatory affairs consulting firm with 100+ remote senior consultants serving pharmaceutical and biotechnology companies across five service pillars: Regulatory Strategy, CMC, Labeling, Advertising & Promotion, and Medical Review & Medical Information.
- Company typePrivate
- Founded1994
- HeadquartersCambridge, United States
- Headcount11–50
- GTM typeB2B
- OfferingServices
What Opus Regulatory does
Opus Regulatory, LLC is a Boston-headquartered regulatory affairs consulting firm serving pharmaceutical and biotechnology organizations. The company operates through five service pillars: Regulatory Strategy, CMC (Chemistry, Manufacturing, and Controls), Labeling, Advertising & Promotion, and Medical Review & Medical Information. Its workforce is structured as 100+ full-time remote-based consultants with an average tenure of 17 years, the majority at Director level or above, positioning Opus as a senior practitioner pool for project engagements rather than a junior-staffing model.
The firm's revenue model is professional services: client engagements are quoted, project-based, and sold through direct enterprise field sales. Opus complements advisory work with a proprietary educational platform that includes the Global Regulatory Labeling Symposium, the PERI Global Labeling & Regulatory Symposium (co-hosted with PERI), and the Opus Insights webinar series covering topics such as CCN Standards and Target Product Profile/Target Product Label. Public pricing for educational programs spans $79 to $5,985 per ticket. The firm claims a global delivery footprint with explicit USA and Europe coverage, and maintains a partnership ecosystem across the regulatory affairs industry's primary bodies—PERI, RAPS Philadelphia, DIA, and FDLI.
Leadership is concentrated around CEO Sidnee Pinho (30+ years biopharma experience), Interim CHRO Olena Maleckyj (licensed pharmacist, 30+ years HR), VP Finance Scott Pano, and four Practice Leaders (Joel Davis, Kim Raymer, Brandon Stempo, Heta Zaveri) covering the five service pillars. No funding rounds, acquisitions, M&A activity, patents, or AI/ML capabilities are disclosed in the available data. The combination of senior-only staffing, named-practice accountability, and a recurring content/education engine is the most distinctive structural feature of the business.
Opus Regulatory firmographics
Firmographics- Name
- Opus Regulatory
- Legal name
- Opus Regulatory, LLC
- Website
- https://opusregulatory.com
- Company type
- Private
- Founded year
- 1994
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Opus Regulatory is a Boston-based regulatory affairs consulting firm with 100+ remote senior consultants serving pharmaceutical and biotechnology companies across five service pillars: Regulatory Strategy, CMC, Labeling, Advertising & Promotion, and Medical Review & Medical Information.
- Ownership category
- akta.pro rank
Opus Regulatory industry classification
Industry- Product category
- Pharmaceutical Regulatory Affairs Consulting
- NAICS
- Management, Scientific, and Technical Consulting Services (5416)
- akta.pro primary industry
- Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA) (HLAGAKAA)
- akta.pro secondary industries
- Regulatory Operations & Publishing (eCTD, RIM, Submission Management) (HLAGAKAC), Regulatory Strategy & IND/NDA/BLA Submissions Support (HLAIALAH)
Keywords
Where Opus Regulatory is headquartered
LocationHeadquarters
- HQ city
- Cambridge
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Opus Regulatory business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Marketing or Sales, Operations, Technology or R&D, Infrastructure
Revenue model
- Regulatory Affairs Consulting Services: Project-based consulting services providing regulatory strategy, CMC, labeling, advertising/promotion, and medical review expertise to pharmaceutical and biotechnology companies. Services are tailored to client needs across all stages of drug development.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| One time/ perpetual license | Pay-as-you-go | Workshop + Symposium: $2,795 USD |
| One time/ perpetual license | Pay-as-you-go | Symposium Only: $1,995 USD (Sale: $1,795) |
| One time/ perpetual license | Pay-as-you-go | Workshop Only: $850 USD (Sale: $650) |
| Subscription | Pay-as-you-go | Group Rate (4+ people): $5,985 USD |
| One time/ perpetual license | Pay-as-you-go | Webinar Individual: $79 |
| One time/ perpetual license | Pay-as-you-go | Webinar Group: $249 |
Go-to-market motion1 record
Distribution channels2 records
Marketing channels4 records
Opus Regulatory product offering
Product offeringCore offering
Opus Regulatory is a niche consulting firm that provides regulatory affairs services to pharmaceutical and biotechnology companies across five pillars: Regulatory Strategy, Regulatory CMC, Labeling, Advertising & Promotion, and Medical Review & Medical Information. The firm delivers these services through a remote team of more than 100 full-time consultants, offering fill-the-gaps staffing, functional outsourcing, and project-based regulatory support across all stages of drug development.
Product overview
Opus Regulatory is a niche regulatory affairs consulting firm offering five integrated core service pillars: Regulatory Strategy, Regulatory CMC (Chemistry, Manufacturing, and Controls), Labeling, Advertising & Promotion (Ad Promo), and Medical Review & Medical Information. The firm operates through its Opus Insights education arm, which delivers the Global Regulatory Labeling Symposium (its own annual event) and partners with PERI for the PERI Global Labeling & Regulatory Symposium. Opus Insights also produces webinars including the CCN Standards series and TPP/TPL sessions. The consulting services provide fill-the-gaps staffing, functional outsourcing, and critical needs support for pharmaceutical and biotechnology companies navigating regulatory requirements across the product lifecycle.
Differentiator
Problem solved
Functional benefit
Products and services
- Regulatory Strategy
Quantifiable outcome
- Team satisfaction with consultant expertise and collaborative personalities
- +2 more outcomes
Companies that use Opus Regulatory
Customer profileNamed customers2 records
Segments3 records
Ideal customer profiles3 records
Opus Regulatory technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Opus Regulatory partnerships and signals
Strategic signalPartnerships
Five partnerships are on record, tiered core and minor.
- PERI (Pharmaceutical Education and Research Institute, Inc.)coreContinued partnership for the PERI Global Labeling & Regulatory Symposium held in Washington, DC. Opus Regulatory co-developed and presented the comprehensive two-day labeling education program featuring interactive presentations, roundtable discussions, case studies, and collaborative sessions.
- PERI (Pharmaceutical Education and Research Institute, Inc.)coreOpus Regulatory developed and presented the PERI Global Labeling & Regulatory Symposium in partnership with PERI. The symposium provides comprehensive labeling education exploring fundamental and specialized concepts including current events and new regulatory initiatives. Faculty includes experts from pharmaceutical companies, thought leaders, academics, and consultant presenters.
- RAPS (Regulatory Affairs Professionals Society) Philadelphia ChapterminorOpus Regulatory sponsors and presents at RAPS Philadelphia Chapter events including networking events and educational sessions on regulatory labeling and ad promo strategy alignment.
- DIA (Drug Information Association)minorOpus Regulatory exhibits at DIA conferences including the Global Annual Meeting, Global Labeling Conference, and Advertising & Promotion Conference. These industry events provide opportunities for networking and brand visibility.
- FDLI (Food and Drug Law Institute)minorOpus Regulatory is a Gold Sponsor of the FDLI Advertising & Promotion for Medical Products Conference, connecting with industry leaders, legal minds, and regulatory professionals on the evolving regulatory landscape.
Scale indicators3 records
Recent moves6 records
Expansion highlights5 records
Opus Regulatory competitors and assessment
Company assessmentDirect peers
- ProPharma Group: ProPharma Group is a specialist pharma services firm offering regulatory affairs, compliance, and pharmacovigilance consulting to pharma and biotech sponsors — directly overlapping Opus's regulatory strategy, CMC, and labeling practices.
- Lachman Consultants: Lachman Consultants is a long-standing regulatory CMC and compliance consulting firm serving pharma/biotech — comparable to Opus in CMC, regulatory strategy, and GMP/compliance functional outsourcing to the same client base.
- Halloran Consulting Group: Halloran is a life sciences consulting firm providing regulatory, quality, and clinical development consulting to pharma and biotech sponsors — directly competitive in regulatory affairs and quality/CMC functional outsourcing engagements.
- NSF (formerly NDA Group): NSF's pharma services business (formerly NDA Group / NLP) provides regulatory affairs, CMC, and drug development consulting to pharma clients across the US and Europe — closely comparable in scope, modality, and client type to Opus.
- Biologics Consulting Group: Biologics Consulting Group is a regulatory affairs and product development consulting firm specializing in biologics and complex therapies — closely comparable to Opus's biotech client segment and submission strategy work.
Broad incumbents
- Parexel International: Parexel is a top-3 global CRO with a dedicated regulatory consulting practice covering strategy, submissions, and labeling — competes with Opus for regulatory outsourcing dollars but as part of a much broader clinical-focused platform.
- IQVIA: IQVIA is the largest CRO with embedded regulatory affairs, CMC, labeling, and safety services — a broad incumbent that overlaps Opus's pillars but at significantly greater scale and with technology-enabled tooling.
- ICON plc: ICON is a leading global CRO with a regulatory and drug development services portfolio — competes with Opus in regulatory strategy, submissions, and labeling outsourcing as part of a broad clinical services platform.
Emerging players
- RJM Group: RJM Group is a regulatory and quality consulting firm serving mid-sized pharma and biotech — a smaller, more regional player competing with Opus for functional outsourcing and ad/promo review projects.
Others
- DIA (Drug Information Association): DIA is the leading industry association for regulatory and clinical professionals — not a competitor but an ecosystem partner whose Global Labeling and Ad/Promo conferences Opus sponsors to drive brand and lead generation.
Market position
Strengths5 records
Weaknesses4 records
Competitive moat3 records
Key risks5 records
Key highlights7 records
Customer concentration
Opus Regulatory social profiles
Digital presenceOpus Regulatory financial estimates
Financial estimateRevenue estimate
Valuation estimate
Opus Regulatory leadership team
Management profileNumber of profiles
Profiles8 records
Opus Regulatory funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Opus Regulatory 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 Opus Regulatory
What does Opus Regulatory do?
Opus Regulatory is a niche consulting firm that provides regulatory affairs services to pharmaceutical and biotechnology companies across five pillars: Regulatory Strategy, Regulatory CMC, Labeling, Advertising & Promotion, and Medical Review & Medical Information. The firm delivers these services through a remote team of more than 100 full-time consultants, offering fill-the-gaps staffing, functional outsourcing, and project-based regulatory support across all stages of drug development.
Is Opus Regulatory a public or private company?
Opus Regulatory is a private company. It is classified as management employee owned and is currently operating.
When was Opus Regulatory founded?
Opus Regulatory was founded in 1994. It employs 11 to 50 people.
Where is Opus Regulatory based?
Opus Regulatory is headquartered in Cambridge, United States, in the North America region.
How does Opus Regulatory make money?
One revenue line is on record: regulatory Affairs Consulting Services.
Who are Opus Regulatory's main competitors?
Direct peers on record are ProPharma Group, Lachman Consultants, Halloran Consulting Group, NSF (formerly NDA Group) and Biologics Consulting Group. Broad incumbents are Parexel International, IQVIA and ICON plc. RJM Group is listed as an emerging player. DIA (Drug Information Association) is listed as an others.
Does Opus Regulatory have an API?
No public API is recorded for Opus Regulatory.
What industry is Opus Regulatory in?
Opus Regulatory's product category is Pharmaceutical Regulatory Affairs Consulting. Its primary akta.pro industry code is HLAGAKAA, Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA), with a secondary code of HLAGAKAC, Regulatory Operations & Publishing (eCTD, RIM, Submission Management). Its NAICS code is 5416.