Advisory, Consulting
& Project Management

Perigord’s Advisory, Consulting and Project Management team provides supply chain programming, packaging technology and design, business process, supplier qualification and logistics planning across all areas of the packaging artwork/labelling supply chain from late stage 2 clinical to commercialisation.

Digitising the supply chain

Start with the end in mind

The Life Science industry is one of the most highly regulated in the world. From product research and development, through initial commercialisation, and long after the product reaches store shelves, companies must overcome complex hurdles.


Managing the challenges of supply chain regulation, CMO selection and qualification, quality and process control, marketing and communications are complex and expensive. Businesses need advisors with experience and insight they can trust and that can help them navigate the complexities – this is where Perigord excels.

Getting things right

The Life Science industry is one of the most highly regulated in the world. From product research and development, through initial commercialisation, and long after the product reaches store shelves, companies must overcome complex hurdles.

Managing the challenges of supply chain regulation, CMO selection and qualification, quality and process control, marketing and communications are complex and expensive. Businesses need advisors with experience and insight they can trust and that can help them navigate the complexities – this is where Perigord excels.

Knowledge
experts in

Perigord’s Advisory, Consulting and Project Management team guides clients on the journey to commercialisation helping them overcome challenges and bring their ambition to life.


Our subject matter experts’ deep knowledge of the Life Science industry supply chain positions them perfectly to deliver real insight, creative and functional solutions that help our clients to build sustainable supply chains that bring products to market quicker.

Packaging technology

Primary & secondary packaging: identification, development & qualification e.g. human factors qualification support (child resistance, senior friendly, patient use accommodation, therapy compliance) due diligence for all packaging development documentation requirements (compliance, qualification & validation)

Portfolio and pack optimisation

SKU reduction/standardisation & COG’s reduction, improved OEE & cycle time, capacity release, waste reduction, portfolio harmonisation, material specification harmonisation

Supplier qualification

Supplier manufacturing/ technical capabilities, CMO/vendor audits quality & security, financial & commercial suitability assessment, manufacturing capability reviews, environmental & employee welfare standards verification

Supply chain programming

CMO selection, due diligence, client technical representation, end-to-end technical project oversight, packaging component & process development support, component manufacturing vendor selection, packaging cost improvement identification, packaging platform/ standardisation opportunities

Logistics planning

Third-party logistics (3PL) identification, selection, qualification, screening & engagement, 3PL oversight for transit pack development, testing & qualification, including distribution qualification (ambient and cold chain)

Managed Services

Perigord can help businesses focus and efficiently manage resources and non-core activities by supporting and managing large non-core multi-disciplinary supplier relationships. Read more.

Business process

End-to-end labelling process development & improvement, end-to-end launch process development & planning, artwork process development, improvement & mapping, new product packaging development & qualification process, co-development process development & improvement, process mapping

Product, brand and
packaging design

Brand strategy, brand & packaging architecture,  identity & brand development, product branding & packaging design,  marketing collateral creation,  campaign launch strategy

Case Study 1

GLOBAL LEADER IN DEVELOPMENT OF ANTI-CANCER THERAPIES

Pre-commercial Pharmaceutical Company

Our client was entering Stage 3 drug development moving toward Health Authority submission and had no artwork development process in place to ensure compliant creation of artwork mockups to support regulatory submission and eventual production of printed packaging components for product launch.

Perigord implemented a three-step plan to:
  • Process Audit and future process design: Perigord identified a high-level future process and required supporting documentation.
  • “To be” Process Development: Present and agree the process with client stakeholders. 
  • Implementation project plan creation: for completion of activities supporting regulatory submission and product launch.
Delivery
  • A detailed labelling and artwork process flow
  • A RACI chart listing each activity on the process flow
  • A fully developed Standard Operating
  • An implementation plan and schedule
  • Checklists and forms to help ensure quality of inputs

CLINICAL-STAGE BIOPHARMACEUTICAL COMPANY

EU & US Launch Programme

Support for development of submission-ready labelling copy and artwork mock-ups. Our client had no regulatory expertise or experience in the assembly and creation of labelling content and artwork mockups required for centralised submission process for EMA.

Perigord was engaged to:
Create compliant, submission-ready labelling content that was then leveraged as editor’s copy for artwork development. 

Delivery
  • Perigord supplied artwork development to create EMA-compliant printed packaging artwork mockups that were ready for submission to the EMA’s centralised submission process.
  • Submission ready mockups were created to be technically correct in every aspect so that, upon Market Authorisation Approval, the same artworks used as mockups during the submission and review process were acceptable for use as production artworks to create actual printed packaging components.

 Case Study 2

Case Study 2

CLINICAL-STAGE BIOPHARMACEUTICAL COMPANY

EU & US Launch Programme

Support for development of submission-ready labelling copy and artwork mock-ups. Our client had no regulatory expertise or experience in the assembly and creation of labelling content and artwork mockups required for centralised submission process for EMA.

Perigord was engaged to:
Create compliant, submission-ready labelling content that was then leveraged as editor’s copy for artwork development. 

Delivery
  • Perigord supplied artwork development to create EMA-compliant printed packaging artwork mockups that were ready for submission to the EMA’s centralised submission process.
  • Submission ready mockups were created to be technically correct in every aspect so that, upon Market Authorisation Approval, the same artworks used as mockups during the submission and review process were acceptable for use as production artworks to create actual printed packaging components.