Trevor Nichols

Trevor Joined Domino in 1991 as Service Engineer, later rising to the position of Senior Service Engineer. He then moved into the commercial side of Domino as a Sales Executive. After four years as an Area Account Manager, Trevor was promoted to Laser Business Development Manager in 1993 and since then has held various Business Development Management roles, including UK Life Sciences Sector Manager, within Domino UK. He is currently the UK Product & Project Manager bringing a wealth of knowledge around the technical, commercial and practical deployment of coding and marking technology.

March 28, 2018

Label serialisation – choosing the correct coding technology for the US DSCSA compliance

Medicines for the US market are predominantly packed in bottles, with statutory information printed on labels affixed to these bottles. As Pharmaceutical manufacturers are gearing up to meet the DSCSA...

BLOG

October 25, 2016

The Changing Face of Pharmaceutical Packaging

$80 billion. That’s how much the global pharmaceutical industry is predicted to be worth by 2020. And it’s no surprise. Packaging has a crucial role in pharma and must adhere to strict standards and regulations. Few other consumables are as potentially harmful.

BLOG

August 26, 2016

How Domino’s Pharma Laser gets you ready for item-level serialisation

The pharmaceutical industry faces strict regulations to ensure safety. Item-level serialization, now EU law, helps prevent mistakes like incorrect dosage or wrong ingredients. Learn how to overcome coding challenges and ensure compliance to avoid litigation, reputational damage, and safety risks.

BLOG

August 02, 2016

8 Trends To Watch in Pharmaceutical Packaging

Blister packaging is on the front line of the fight to improve dosage compliance, because it makes it easier for patients to keep track of their dosing, dosage days can be printed on the packaging. Blister packaging also protects medication and can be customised, so you can see why it is the world’s second best-selling pharmaceutical packaging.

BLOG

July 21, 2016

GS1 standards in the pharma industry

The legislative move to item-level serialisation is a massive operational shake-up in the pharmaceutical industry. As the sector squares up to the challenge, EFPIA have advocated the use of GS1 standards as a framework to track medications through the supply chain. Here’s what it means for your coding processes.

BLOG

April 27, 2016

What’s the best technology for adding unique codes to pharmaceutical packaging?

If you haven’t already, now is the time to begin planning for item-level serialisation in the pharmaceutical industry. Soon you will be legally obliged to make sure every packet or bottle of prescribed medication carries the correct coding information. Here’s how thermal inkjet printers can help.

BLOG

December 01, 2015

A complete guide to item-level serialisation in the pharma industry

The biggest legislative change in the history of the pharmaceutical industry has been given the green light by the European Commission. Here’s everything you need to know about preparing for the move to item-level serialisation.

BLOG

September 25, 2015

UDI in the NHS: what suppliers should know

From pharmaceuticals to surgical equipment, every product being used in the NHS should have a unique device identification (UDI) number. As a supplier, the time to get your coding standards in check is now.

BLOG

August 07, 2015

Print and apply labelling in the pharmaceutical industry

The pharmaceutical industry is facing one of its biggest challenges. The legislative move to item-level serialisation is looming. There’s no doubt that print and apply labelling systems have come a long way in the last twenty years, but can manufacturers trust them for their sternest operational challenge yet?

BLOG

June 09, 2015

How do you stop falsified products entering global supply chains?

We are living in a world of global supply chains. And when everything from your body wash to your burgers could have come from the other side of the world, product traceability is vital. So how is it done? And how do you try to stop the widespread and dangerous problem of falsified products?

BLOG

Trevor Nichols

Articles from Trevor Nichols