Information

From Planning to Execution in Life Science

Why projects stall and how to
move forward
.

In Life Science, planning is rarely the problem. Organizations invest significant time in strategies, roadmaps, validation plans and regulatory assessments. Yet many projects still struggle when it’s time to move from plan to execution. Timelines slip, ownership becomes unclear, and well-designed plans fail to translate into real progress.

So why does this happen and what can be done differently?

In this article, we explore why projects stall and share practical, experience-based tips on how to turn strategies into real, compliant execution.

Read the full article and learn how to move from planning to execution.

Our Expertise

Could QA IT have prevented the Chernobyl disaster?

What if modern QA IT principles as risk assessment, data integrity and validated proof had been applied in the Chernobyl control room in 1986?

Using this thought experiment, we explore what QA IT really does today: making risks visible, building quality into systems from the start, and demanding evidence instead of assumptions.

Read the full article and explore why QA IT is critical in today’s GxP and cloud-based environments. 

Join our upcoming webinar tomorrow!
Register below and secure your spot.

Our Services

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practical tips on how to move forward with greater clarity
and impact.

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We Welcome

Welcome Anneli Häkkinen
– Head of Quality Assurance

We are pleased to welcome Anneli Häkkinen as our new Head of Quality Assurance at PharmaRelations.

Anneli brings extensive experience in quality management within the Life Science industry and will play an important role in further strengthening our quality framework and supporting our clients across the Nordics.

Read more about Anneli

Anneli Häkkinen
Head of Quality Assurance
+46 70 165 22 42
Email me

Here are three practical principles to help turn
strategy into compliant, effective action.

1️⃣ Plan for Execution. Not Just Approval.

In Life Science, significant effort is often spent creating plans that can be approved. However, real success depends on how executable those plans are in daily operations.

2️⃣ Integrate Quality and Regulatory from the start.

Adding QA or Regulatory late in a project often leads to delays, rework and
unnecessary friction.

3️⃣ Ensure the Right Competence at the Right Phase.

Projects frequently stall due to competence gaps during critical phases.

Want to explore how to strengthen execution in your organisation?
Let’s start the conversation. Contact our team.

Events and Webinars

WEBINAR | QA IT Unplugged: The Most Common Mistakes and How to Avoid Them
Tomorrow March 20

This webinar demystifies what QA IT is in GxP environments. Participants will learn from real‑life pitfalls instead of paying for
them later, and gain insight into where organizations typically struggle
when implementing and maintaining computerized systems.

Register for the event

 

PharmaRelations speaker at "The future of
Swedish and Danish Life Science
" on April 23.

The topic of the session is: Where Science Meets Digital:
Building the Next Generation Workforce in Danish and
Swedish Life Sciences.

Read more here

Career opportunities

Career opportunity | Nordic Head of
Pharmacovigilance and Safety

NORDICS

We are looking for a dynamic and experienced professional to join
our team as the Nordic Head of Pharmacovigilance and Safety.
This is a leadership position that combines strategic oversight,
business development, and team leadership.

Apply for the job

 

Career opportunity | Business Developer and
Consultant Manager

NORWAY

We are now looking for a Business Developer and Consultant Manager to support our Quality Assurance, Regulatory Affairs, Pharmacovigilance business in Norway.

Apply for the job

We want to be the Best Place to Work in Nordic Life Science.
Join the PharmaRelations family, see our open positions at
PharmaRelations.com

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