Services

  • Our Services

Expert Regulatory Services

MHRA & EU License Set Up

Guidance for WDA, MIA, PLPI, MS, and Controlled Drugs licensing in the UK and EU.

Contract QP, RP & RPi

Short- and long-term contract services from a qualified team at competitive prices.

Medical Device Registration

Comprehensive regulatory support, technical file preparation, and UK RP services.

GXP Audits

Global audit services for API units, plants, logistics sites, and laboratories.

PDE & HBEL Reports

Impurity risk assessments by certified toxicologists for regulatory compliance.

Sourcing Services

Strong networks to help source dossiers, partners, and manufacturers.

Pharma Limited

MD

Prompt Response and Professional Service

Years of Experience
0
  • FAQ Question

Explore Answers to Your Common Questions

1. What industries do you serve with your regulatory and compliance services?

We cater to pharmaceutical, medical device, and food supplement industries, offering solutions tailored to each sector's regulatory needs.

2. Do you provide support for MHRA and EU license applications?

Yes, we specialize in setting up licenses such as WDA, MIA, PLPI, MS, and Controlled Drugs for clients in the UK and EU.

3. Can you assist with global audits and compliance?

Absolutely, our qualified auditors conduct GXP audits worldwide for API units, manufacturing plants, logistics sites, and laboratories.

  • Start a Conversation

Get in Touch Now

Need personalized advice? Our dedicated team is here to assist you. Reach out today for expert support and tailored solutions to meet your needs.

    Email Address

    info@pharmagxp-co-uk.preview-domain.com

     

    Phone

    +44 745 930 2113

    Office Location

    203 Camrose Avenue
    Edgware HA8 6DG