Training + Consultancy = LASTING IMPACT

Why consultancy?

After a training session, this question often arises:

❝ How do we ensure that this knowledge translates into better processes, compliant behaviour and lasting improvements? ❞

That is where our added value lies.

Our consultants combine in-depth knowledge of GMP regulations with years of practical experience in production, quality and laboratory environments. This enables us to support organisations with both content-related issues and the actual implementation on the shop floor.

Below is a selection from our wide-ranging expertise:

When can you call on us?

• After a training course to implement acquired knowledge

• When preparing for an inspection or audit

• When introducing new GMP guidelines

• When facing challenges relating to Annex 1 or aseptic working

• During the improvement of quality processes

• Where there are validation or documentation issues

• When additional capacity or specialist knowledge is required

Our approach

1. Analysis: we identify processes, risks and areas for improvement.

2. Advice: practical recommendations tailored to your organisation.

3. Implementation: on-the-job guidance and support for teams.

4. Assurance: embedding knowledge, behaviour and processes to ensure lasting results.

What are the benefits?

• Faster implementation of training results

• Improved GMP compliance

• Fewer non-conformities and recurring issues

• Greater sense of ownership within teams

• More efficient processes

• Solutions that can be applied instantly

Why Biotech Training Facility?

✔ A unique combination of training and consultancy

✔ Practical experience in pharmaceutical manufacturing and laboratories

✔ Specialists in GMP, Annex 1 and aseptic practices

✔ Focus on practical applicability

✔ Support from analysis through to implementation