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cro cdmo — illustrative research and development scene 1
cro cdmo — illustrative research and development scene 2
cro cdmo — illustrative research and development scene 3
cro cdmo — illustrative research and development scene 4
cro cdmo — illustrative research and development scene 5
cro cdmo — illustrative research and development scene 6
TRUE RESEARCH PEPTIDES LABS

CRO & CDMO development

Research, development and manufacturing coordination with agreed milestones and acceptance criteria.

Research materialsCustom synthesisOEM · ODM · CRO · CDMO

Research, development and manufacturing coordination with agreed milestones and acceptance criteria.

Turn the project objective into deliverables

A research program needs an answerable question and a defined output. A development and manufacturing program additionally needs a process, specification and transfer plan. Discuss the sequence or formulation, known technical issues, planned trials, target amount and the evidence needed at each review point.

CRO enquiries

Define the research question, experimental scope, material needs and the reporting format. Agree which work is exploratory and which has formal acceptance criteria.

Development review

Set sample objectives, analytical needs, prototype tests and decision points before committing to a manufacturing route.

CDMO enquiries

Connect process development and scale-up with the target specification, manufacturing documentation and quality responsibilities.

Project ownership

Agree confidentiality, intellectual property, data access, subcontracted work and the responsibilities of each organization.

A research-stage result does not automatically establish commercial reproducibility or suitability for a regulated application. The project plan should identify the evidence that needs to be repeated or extended as the scale, process or intended category changes.

Prepare your project brief

  • Sequence, structure or formulation objective.
  • Current development stage and known constraints.
  • Research questions and measurable deliverables.
  • Prototype and production quantity scenarios.
  • Analytical, documentation and transfer requirements.

Send your requirements ↗

From brief to project delivery

  1. 01

    Gather requirements

    Define material identity, product format, quantity, target market and acceptance requirements.

  2. 02

    Technical review

    Assess feasibility, project risks and the work needed to answer the brief.

  3. 03

    Prototype sampling

    Prepare an agreed development sample for evaluation.

  4. 04

    Evaluate the sample

    Review analytical results, format performance and the changes needed.

  5. 05

    Confirm the specification

    Agree the material, presentation, acceptance criteria and documentation scope.

  6. 06

    Develop artwork

    Review branded labels, packaging information and destination-market requirements.

  7. 07

    Approve packaging

    Confirm the container, closure, carton and approved artwork.

  8. 08

    Confirm project terms

    Agree the scope, quotation, milestones and responsibilities.

  9. 09

    Production and review

    Execute the agreed scope and review the applicable batch records.

  10. 10

    Delivery coordination

    Confirm documentation, transport requirements and the handover information.

MANUFACTURING FOOTAGE

A closer look at the workshop.

A CLEAR BRIEF IS THE FIRST STEP

Start your next peptide project.

Tell us the material, specification, quantity and destination market.

Request a quotation ↗