Regulated Life Sciences (RLS)

Navigating complexity in Regulated Life Sciences

At DAQUMA, we combine deep domain expertise in Commercial, Clinical, and Regulatory Affairs with strong capabilities in data, validation, and GenAI. Our flexible and highly skilled consultants help life science organizations solve complex regulatory challenges, optimize processes, and accelerate innovation — all while ensuring compliance and quality across the entire value chain.

What is RLS at DAQUMA?

At DAQUMA, Regulated Life Sciences is where domain expertise meets execution power. We help pharmaceutical, biotech, and medtech companies navigate the complex landscape of regulations, data integrity, and digital transformation - with a clear focus on delivering results.

By working across Commercial, Clinical, and Regulatory Affairs, we enable clients to:

Adapt quickly to evolving compliance requirements
Optimize systems and processes
Leverage data and technology to drive smarter decisions

Our RLS domain naturally complements DAQUMA’s broader capabilities in Data, Quality, and Validation, making us a powerful partner for end-to-end consulting across the life science value chain.

Our focus areas

Commercial

We support commercial teams with CRM best practices, HCP data optimization, and commercial ops execution.

We help clients:

Adopt Veeva CRM best practices
Optimize HCP research using OpenData & OneKey
Improve CRM data quality, integration, and reporting

Clinical

We help clinical teams ensure data integrity, system compliance, and smooth migration across platforms.

We help clients:

Define and implement data governance frameworks
Design compliant workflows and manage clinical data migrations
Implementation and configuration of systems like eTMF, CTMS, and DCT platforms

Regulatory Affairs

We support regulatory functions with technology-driven compliance and smarter submissions.

We help clients:

Navigate global regulatory requirements
Leverage IT to enhance efficiency and automation
Implement data governance and quality frameworks

Consultant roles include

Commercial Business analyst / PM
Vault CRM Consultant
Veeva PromoMats Consultant
Veeva OneKey / Opendata Consultant
Tech PM, Commercial specialist

Configuration Specialist
Clinical Data Stewards
Veeva Clinical Platform specialist
Clinical System Migration PM
Tech PM, Clinical specialization

Configuration Specialist
RA Systems Development Experts
Regulatory Affairs Specialist
Data Steward
Submission Manager

Why DAQUMA?

We know the life science industry — and we understand how to get things done within it.

Our consultants bring a rare combination of regulatory, clinical, and commercial know-how, paired with strong capabilities in data, validation, and technology. Whether it’s rolling out a new CRM, navigating a global regulatory change, or managing high-stakes clinical data migrations, we step in as hands-on partners who deliver.

What sets us apart:

Deep domain expertise across Commercial, Clinical, and Regulatory Affairs
Cross-functional mindset that bridges Management, Data, and Quality
Flexible delivery - from strategic advice to hands-on delivery inside your teams
Trusted by clients to lead complex, high-impact initiatives

Our mission is simple: help life science companies thrive in complexity — and move faster with confidence.

Let’s talk about your next challenge.

We’re happy to share how we can support you in Regulatory, Clinical, or Commercial transformation — no strings attached.

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