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SFL Regulatory Affairs & Scientific Communication

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uuid002dcf4

Namestring
SFL Regulatory Affairs & Scientific Communication
Legal namestring
Veristat, LLC
Company typeenum
Private
Founded yearint
2009
Descriptiontext

SFL Regulatory Affairs & Scientific Communication (Solutions for Life Science) was a Basel, Switzerland-based regulatory and scientific consulting firm serving pharmaceutical, biotechnology, medical device, and rare disease developers across the product lifecycle. Its service portfolio spanned regulatory strategy and submissions, pharmacovigilance, market access and reimbursement, supply chain support for drugs/biologics/devices, healthcare compliance, and quality assurance — delivered on a professional services, quote-based engagement model typical of mid-tier regulatory consultancies. The firm was structured as a boutique, with primary targeting of pharma and biotech clients and secondary targeting of medical device/IVD companies; pricing was not publicly disclosed.

SFL has been acquired by and fully integrated into Veristat, LLC, a US-based private CRO. The SFL entity no longer operates independently; its Basel office now functions as Veristat's European headquarters. The integration extends the combined organization's offering from regulatory consulting into full-service clinical operations, biometrics, medical writing, and therapeutic-area solutions (oncology, neurology, infectious disease, cardiovascular, biologics including cell/gene therapy, rare disease/pediatric, decentralized trials, and natural history studies). Marketing is conducted through industry events, webinars, case studies, blog/library content, newsletters, and social channels (LinkedIn, Twitter/X, Facebook, YouTube), with all demand conversion routed through direct enterprise sales and an RFP intake flow. No AI/ML, API, SDK, or proprietary technology assets are disclosed; the moat rests on regulatory expertise, integrated cross-functional packaging, and the consulting talent base.

Short descriptiontext

SFL Regulatory Affairs & Scientific Communication was a Basel-based regulatory and scientific consulting firm for pharma, biotech, medical device, and rare disease developers; it has been acquired by and fully integrated into US-based CRO Veristat.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBasel, Switzerland
HQ citystring
Basel
HQ countrystring
Switzerland
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
regulatory affairs consulting, pharmacovigilance services, clinical development support, market access reimbursement, healthcare compliance advisory
Industry1 code
1Pharmacovigilance Quality & Compliance (PV audits, QPPV support, PSMF)
CodeHLAGAKAHPrimaryYes
NAICS code2 codes
  • Management Consulting Services54161
  • Management, Scientific, and Technical Consulting Services5416
SIC code1 code
  • Services-Management Consulting Services8742
Product category
Regulatory Affairs Consulting
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model5 records
1Regulatory Consulting Services
TypeProfessional Services
Description

Provides regulatory strategy, consulting, and submission services for clinical development programs and marketing applications throughout the product lifecycle.

veristat.com
2Pharmacovigilance Services
TypeProfessional Services
Description

Safety management services throughout the product lifecycle, including clinical trial safety, data monitoring committees, and medical monitoring.

veristat.com
3Market Access and Reimbursement
TypeProfessional Services
Description

Strategic consulting to secure early access and reimbursement for drugs and biologics.

veristat.com
4Supply Chain Services
TypeProfessional Services
Description

Expert services to establish and maintain seamless supply of commercial and investigational products for drugs, biologics, and medical devices.

veristat.com
5Healthcare Compliance Services
TypeProfessional Services
Description

Strategic expertise to ensure compliant relations and promotional materials for healthcare companies.

veristat.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Marketing or Sales, Technology or R&D, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

SFL (now operating as Veristat) provides integrated consulting solutions for life sciences companies across the development and commercialization lifecycle. Core offerings include regulatory affairs strategy, pharmacovigilance, market access and reimbursement consulting, supply chain services, healthcare compliance advisory, and quality assurance/compliance services for pharmaceutical, biotechnology, and medical device clients.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

SFL Regulatory Affairs & Scientific Communication (now part of Veristat) offers an integrated suite of clinical development and regulatory affairs consulting services. The portfolio spans core regulatory services (Regulatory Affairs, Pharmacovigilance, Market Access/Reimbursement, Supply Chain, Healthcare Compliance, and Quality Assurance & Compliance), supported by strategic service modules (Strategic Consulting, Clinical Operations, Medical Affairs, Medical Writing, Biometrics, Regulatory Writing, and Resourcing/FSP). Solutions are organized around key therapeutic approaches including Biologics (Cell and Gene Therapies, Vaccine Trials), Rare Diseases (including Pediatric), Decentralized Trials, Rescue Trials, and Natural History Trials. The company provides integrated consulting solutions across the entire development and commercialization lifecycle, from program design through full-service clinical trial execution and therapy commercialization.

Product and service12 records
1Regulatory Affairs
CategoryRegulatory Consulting
Description

Regulatory expertise and strategy throughout all phases of clinical development into commercialization, including regulatory consulting for program and trial design, marketing applications, CMC, agency meetings, and regulatory publishing.

2Pharmacovigilance
CategorySafety and Pharmacovigilance
Description

Safety management throughout the product lifecycle, including clinical trial safety, data monitoring committees, and medical monitoring.

3Market Access and Reimbursement
CategoryMarket Access Consulting
Description

Strategic consulting to apply knowledge and insights to secure early access and reimbursement for drugs and biologics.

4Supply Chain Services
CategorySupply Chain Consulting
Description

Expert services to establish and maintain seamless supply of commercial and investigational products for drugs, biologics, and medical devices.

5Healthcare Compliance
CategoryCompliance Consulting
Description

Strategic expertise to ensure compliant relations and promotional materials for healthcare products.

6Quality Assurance and Compliance
CategoryQuality Assurance Consulting
Description

Quality compliance services from quality management systems (QMS) establishment to quality oversight of marketed products.

7Biologics Solutions
CategoryTherapeutic Solutions
Description

Full-service CRO solutions for biologics development, including cell and gene therapies and vaccine trials.

8Rare Diseases Solutions
CategoryTherapeutic Solutions
Description

Specialized solutions for rare disease clinical trials, including pediatric clinical trials.

9Clinical Operations
CategoryClinical Operations
Description

Full-service clinical trial execution including project management, monitoring and site management, patient recruitment, and patient retention and site engagement.

10Biometrics Services
CategoryBiometrics and Data Services
Description

Comprehensive biometrics services including data management, biostatistics, statistical programming, and standards implementation.

11Strategic Resourcing/FSP
CategoryStaffing and Resourcing
Description

Flexible staffing solutions and functional service provider (FSP) resourcing for clinical development programs.

12Decentralized Trials
CategoryTrial Solutions
Description

Decentralized clinical trial solutions enabling remote participation and distributed data collection.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

SFL has been acquired by and integrated into Veristat, creating a combined organization with expanded capabilities in clinical development, regulatory affairs, and market access. The integration enables SFL to better serve clients' clinical development and regulatory affairs needs across the product development lifecycle, from program design to full-service clinical trial execution and therapy commercialization.

Recent move4 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Market position
Competitive moat3 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile4 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

SFL Regulatory Affairs & Scientific Communication

Regulatory Affairs Consultingsfl-services.com

SFL Regulatory Affairs & Scientific Communication was a Basel-based regulatory and scientific consulting firm for pharma, biotech, medical device, and rare disease developers; it has been acquired by and fully integrated into US-based CRO Veristat.

What SFL Regulatory Affairs & Scientific Communication does

SFL Regulatory Affairs & Scientific Communication (Solutions for Life Science) was a Basel, Switzerland-based regulatory and scientific consulting firm serving pharmaceutical, biotechnology, medical device, and rare disease developers across the product lifecycle. Its service portfolio spanned regulatory strategy and submissions, pharmacovigilance, market access and reimbursement, supply chain support for drugs/biologics/devices, healthcare compliance, and quality assurance — delivered on a professional services, quote-based engagement model typical of mid-tier regulatory consultancies. The firm was structured as a boutique, with primary targeting of pharma and biotech clients and secondary targeting of medical device/IVD companies; pricing was not publicly disclosed.

SFL has been acquired by and fully integrated into Veristat, LLC, a US-based private CRO. The SFL entity no longer operates independently; its Basel office now functions as Veristat's European headquarters. The integration extends the combined organization's offering from regulatory consulting into full-service clinical operations, biometrics, medical writing, and therapeutic-area solutions (oncology, neurology, infectious disease, cardiovascular, biologics including cell/gene therapy, rare disease/pediatric, decentralized trials, and natural history studies). Marketing is conducted through industry events, webinars, case studies, blog/library content, newsletters, and social channels (LinkedIn, Twitter/X, Facebook, YouTube), with all demand conversion routed through direct enterprise sales and an RFP intake flow. No AI/ML, API, SDK, or proprietary technology assets are disclosed; the moat rests on regulatory expertise, integrated cross-functional packaging, and the consulting talent base.

SFL Regulatory Affairs & Scientific Communication firmographics

Firmographics
Name
SFL Regulatory Affairs & Scientific Communication
Legal name
Veristat, LLC
Website
https://sfl-services.com
Company type
Private
Founded year
2009
Operating status
Acquired
Headcount range
11–50 employees
Short description
SFL Regulatory Affairs & Scientific Communication was a Basel-based regulatory and scientific consulting firm for pharma, biotech, medical device, and rare disease developers; it has been acquired by and fully integrated into US-based CRO Veristat.
Ownership category
akta.pro rank

SFL Regulatory Affairs & Scientific Communication industry classification

Industry
Product category
Regulatory Affairs Consulting
NAICS
Management Consulting Services (54161), Management, Scientific, and Technical Consulting Services (5416)
SIC
Services-Management Consulting Services (8742)
akta.pro primary industry
Pharmacovigilance Quality & Compliance (PV audits, QPPV support, PSMF) (HLAGAKAH)

Keywords

  • Regulatory affairs consulting
  • Pharmacovigilance services
  • Clinical development support
  • Market access reimbursement
  • Healthcare compliance advisory

Where SFL Regulatory Affairs & Scientific Communication is headquartered

Location

Headquarters

HQ city
Basel
HQ country
Switzerland
HQ region
Europe

Offices1 record

Markets served

SFL Regulatory Affairs & Scientific Communication business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Marketing or Sales, Technology or R&D, Infrastructure

Revenue model

  1. Regulatory Consulting Services: Provides regulatory strategy, consulting, and submission services for clinical development programs and marketing applications throughout the product lifecycle.
  2. Pharmacovigilance Services: Safety management services throughout the product lifecycle, including clinical trial safety, data monitoring committees, and medical monitoring.
  3. Market Access and Reimbursement: Strategic consulting to secure early access and reimbursement for drugs and biologics.
  4. Supply Chain Services: Expert services to establish and maintain seamless supply of commercial and investigational products for drugs, biologics, and medical devices.
  5. Healthcare Compliance Services: Strategic expertise to ensure compliant relations and promotional materials for healthcare companies.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

SFL Regulatory Affairs & Scientific Communication product offering

Product offering

Core offering

SFL (now operating as Veristat) provides integrated consulting solutions for life sciences companies across the development and commercialization lifecycle. Core offerings include regulatory affairs strategy, pharmacovigilance, market access and reimbursement consulting, supply chain services, healthcare compliance advisory, and quality assurance/compliance services for pharmaceutical, biotechnology, and medical device clients.

Product overview

SFL Regulatory Affairs & Scientific Communication (now part of Veristat) offers an integrated suite of clinical development and regulatory affairs consulting services. The portfolio spans core regulatory services (Regulatory Affairs, Pharmacovigilance, Market Access/Reimbursement, Supply Chain, Healthcare Compliance, and Quality Assurance & Compliance), supported by strategic service modules (Strategic Consulting, Clinical Operations, Medical Affairs, Medical Writing, Biometrics, Regulatory Writing, and Resourcing/FSP). Solutions are organized around key therapeutic approaches including Biologics (Cell and Gene Therapies, Vaccine Trials), Rare Diseases (including Pediatric), Decentralized Trials, Rescue Trials, and Natural History Trials. The company provides integrated consulting solutions across the entire development and commercialization lifecycle, from program design through full-service clinical trial execution and therapy commercialization.

Differentiator

Problem solved

Functional benefit

Products and services

  • Regulatory Affairs Regulatory expertise and strategy throughout all phases of clinical development into commercialization, including regulatory consulting for program and trial design, marketing applications, CMC, agency meetings, and regulatory publishing.
  • Pharmacovigilance Safety management throughout the product lifecycle, including clinical trial safety, data monitoring committees, and medical monitoring.
  • Market Access and Reimbursement Strategic consulting to apply knowledge and insights to secure early access and reimbursement for drugs and biologics.
  • Supply Chain Services Expert services to establish and maintain seamless supply of commercial and investigational products for drugs, biologics, and medical devices.
  • Healthcare Compliance Strategic expertise to ensure compliant relations and promotional materials for healthcare products.
  • Quality Assurance and Compliance Quality compliance services from quality management systems (QMS) establishment to quality oversight of marketed products.
  • Biologics Solutions Full-service CRO solutions for biologics development, including cell and gene therapies and vaccine trials.
  • Rare Diseases Solutions Specialized solutions for rare disease clinical trials, including pediatric clinical trials.
  • Clinical Operations Full-service clinical trial execution including project management, monitoring and site management, patient recruitment, and patient retention and site engagement.
  • Biometrics Services Comprehensive biometrics services including data management, biostatistics, statistical programming, and standards implementation.
  • Strategic Resourcing/FSP Flexible staffing solutions and functional service provider (FSP) resourcing for clinical development programs.
  • Decentralized Trials Decentralized clinical trial solutions enabling remote participation and distributed data collection.

Companies that use SFL Regulatory Affairs & Scientific Communication

Customer profile

Segments4 records

Ideal customer profiles4 records

SFL Regulatory Affairs & Scientific Communication technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

SFL Regulatory Affairs & Scientific Communication partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • VeristatflagshipStrategic or Co-development PartnerSFL has been acquired by and integrated into Veristat, creating a combined organization with expanded capabilities in clinical development, regulatory affairs, and market access. The integration enables SFL to better serve clients' clinical development and regulatory affairs needs across the product development lifecycle, from program design to full-service clinical trial execution and therapy commercialization.

Scale indicators1 record

Recent moves4 records

Expansion highlights5 records

SFL Regulatory Affairs & Scientific Communication competitors and assessment

Company assessment

Market position

Competitive moat3 records

Key risks5 records

Key highlights5 records

Customer concentration

SFL Regulatory Affairs & Scientific Communication social profiles

Digital presence

SFL Regulatory Affairs & Scientific Communication financial estimates

Financial estimate

Revenue estimate

Valuation estimate

SFL Regulatory Affairs & Scientific Communication leadership team

Management profile

Number of profiles

SFL Regulatory Affairs & Scientific Communication funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

SFL Regulatory Affairs & Scientific Communication M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about SFL Regulatory Affairs & Scientific Communication

What does SFL Regulatory Affairs & Scientific Communication do?

SFL (now operating as Veristat) provides integrated consulting solutions for life sciences companies across the development and commercialization lifecycle. Core offerings include regulatory affairs strategy, pharmacovigilance, market access and reimbursement consulting, supply chain services, healthcare compliance advisory, and quality assurance/compliance services for pharmaceutical, biotechnology, and medical device clients.

Is SFL Regulatory Affairs & Scientific Communication a public or private company?

SFL Regulatory Affairs & Scientific Communication is a private company. It is classified as unknown and is currently acquired.

When was SFL Regulatory Affairs & Scientific Communication founded?

SFL Regulatory Affairs & Scientific Communication was founded in 2009. It employs 11 to 50 people.

Where is SFL Regulatory Affairs & Scientific Communication based?

SFL Regulatory Affairs & Scientific Communication is headquartered in Basel, Switzerland, in the Europe region.

How does SFL Regulatory Affairs & Scientific Communication make money?

Five revenue lines are on record. Regulatory Consulting Services are the primary driver. The others are pharmacovigilance Services, market Access and Reimbursement, supply Chain Services and healthcare Compliance Services.

Does SFL Regulatory Affairs & Scientific Communication have an API?

No public API is recorded for SFL Regulatory Affairs & Scientific Communication.

What industry is SFL Regulatory Affairs & Scientific Communication in?

SFL Regulatory Affairs & Scientific Communication's product category is Regulatory Affairs Consulting. Its primary akta.pro industry code is HLAGAKAH, Pharmacovigilance Quality & Compliance (PV audits, QPPV support, PSMF). Its NAICS code is 54161 and its SIC code is 8742.

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