Pharma & Biotech Manufacturing Advisory

A clearer path
to the right
CDMO.

Tell us what you need to manufacture. ClearPath CMC gathers quotes from vetted contract development and manufacturing organizations — then adds expert annotations so you can compare with confidence.

Sample quote comparison
ACG
Alcami Group
API synthesis · 12-week lead time
$148,000
Best value
KBI
KBI Biopharma
API synthesis · 10-week lead time
$172,500
CAT
Catalent
API synthesis · 8-week lead time
$201,000
Get Quotes
Community Forum
How It Works
Submit a manufacturing request

Fill in the details below. ClearPath CMC will reach out to our network of CDMOs and return an annotated comparison of quotes, timelines, and capabilities — typically within 3–5 business days.

Your information is confidential and only shared with CDMOs who are a fit for your project.
Community forum

Free to read and participate. Share your experiences — positive or negative — with CDMOs you've worked with. Help others make informed decisions.

Share your experience
MK
M. Kowalski · Formulation Scientist
June 12, 2026
Positive
Solid experience with Lonza for Phase II biologics
We used Lonza's Visp facility for our anti-IL-17 mAb. Communication was consistent, tech transfer went smoothly, and they flagged a potential CMC risk proactively that we hadn't considered. Lead time was 14 weeks as quoted. Would use again for Phase III.
24 6 replies Save
DR
D. Reyes · CMC Director
June 8, 2026
Negative
Significant timeline slippage at a mid-tier CDMO — lessons learned
Won't name them outright but a mid-sized US CDMO caused us a 9-week delay due to equipment scheduling conflicts they didn't disclose upfront. Ask specifically about equipment availability and backup plans before signing. Their project management was also fragmented — we had three different PMs in six months.
41 13 replies Save
SJ
S. Jha · Head of Supply Chain
May 29, 2026
Question
Any experience with sterile fill-finish in India for US IND submission?
We're exploring Divi's or Piramal for our Phase I sterile injectables. Cost looks attractive but want to understand if there are any FDA import alert risks or inspection history concerns I should be aware of. Has anyone navigated this path successfully?
8 4 replies Save
How ClearPath CMC works

A straightforward process — no subscriptions, no vendor lock-in. Getting quotes is free for clients.

01
Submit your request
Tell us what you need: service type, molecule class, scale, timeline, and any regulatory constraints. The more detail you provide, the more accurate and relevant the quotes we return.
02
We gather quotes
We reach out to CDMOs in our network who are qualified for your project. We collect quotes, capacity availability, lead times, and relevant certifications on your behalf.
03
You compare and choose
You receive a structured comparison — price, lead time, regulatory standing, and capabilities — with expert annotations. Select who to engage with, or walk away. Your data stays private.
Free for clients. Always.
ClearPath CMC is funded through introductory fees paid by CDMOs when a client engagement begins — similar to a recruiting platform model. You never pay to receive or compare quotes. The community forum is entirely free and open to anyone in the industry.