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COMPANY RESEARCH

Crystal Pharmatech

Focuses on solid-state R&D, including polymorph, salt, and cocrystal screening, crystallization process development, and structural characterization using complementary techniques.

Company at a glance

Corporate information

Company entity
Crystal Pharmatech
Headquarters / principal office
Cranbury, New JerseySelf-reported location on the company LinkedIn page; regional scope may differ from the legal or global headquarters. ↗
Founded
2010 ↗
Ownership / capital status
PrivateSeries B (disclosed in 2018) ↗
Official corporate reference
https://www.crystalpharmatech.com/ ↗
LinkedIn company page
LinkedIn ↗ ↗
Latest financing / award identified
2018 · Series B · USD 14.5 million ↗

Disclosed in the official company history, with year-level precision only; this does not establish that there was no subsequent financing by the access date.

Profile review: 2026-11-04 · Fields retain their individual source dates. Undisclosed values are not zero; early or historical events do not establish the latest financing. Awards and acquisitions are distinguished from equity rounds.

Disease tags match recorded text mentions and require program-level verification.

Technology, programs & evidence

The group connects candidates with clinical and commercial supply through solid-state, preformulation, oral formulation development, and manufacturing services. Formulation execution entities include CFS and Candoo.

The solid-form screening service page explicitly lists polymorph, salt, and cocrystal screening.

Disclosed structural characterization methods include XRPD, ssNMR, SCXRD, and MicroED. Complementary techniques should be selected for each project.

The current website lists MicroED, XRPD, ssNMR, and SCXRD as structural characterization services.

An April 2026 collaboration announcement with ELDICO disclosed plans to introduce a dedicated ED-1 in Suzhou. The announcement alone does not establish completed acceptance testing.

Program / serviceTarget / indicationRepresentative stageEvidence & scope
Formulation development / contract manufacturing capabilitiesDefined by the client project · Defined by the client projectServices / platformService pages do not establish human evidence for every project
Solid-state R&D capabilitiesDetermined by the submitted sample and research question · Not applicable; service capabilityServices / platformNot applicable; not a human clinical program
MicroED / 3D ED service capabilitiesDetermined by the submitted sample and research question · Not applicable; service capabilityServices / platformNot applicable; not a human clinical program

Related news & literature

Company-name matches are discovery leads; verify entity identity and transaction roles in the original source.

Biotech Assistant · Original commentary · Blog / commentary

How MicroED is Transforming Drug Polymorph Research Workflow

This article explores how Microcrystal Electron Diffraction (MicroED) is set to revolutionize drug polymorph research workflows. Drawing upon recent news, official websites, and LinkedIn updates from Crystal Pharmatech and Eldico, it clearly distinguishes between verified facts, industry viewpoints, and information pending verification.

Same-field reading (not company-specific)
Nature Communications

Peptide–oligonucleotide nanohybrids deliver miRNA to injured bone in rats

A Nature Communications study reports a peptide–oligonucleotide nanohybrid for bone-targeted miR-26a-5p delivery. The original abstract describes reduced GSK-3β expression and stabilization of HIF-1α, supporting coupled bone formation and angiogenesis. Systemic administration limited skeletal and vascular injury in a rat glucocorticoid-induced bone-loss model. This is preclinical miRNA delivery, not oral cyclic peptide therapy or human efficacy evidence.

U.S. Food and Drug Administration

FDA grants accelerated approval for subcutaneous amivantamab combination in selected head and neck cancers

FDA granted accelerated approval to amivantamab and hyaluronidase-lpuj for adults with recurrent or metastatic head and neck squamous cell carcinoma after platinum chemotherapy and an anti-PD-(L)1 antibody. HPV-associated oropharyngeal cancer is excluded. In the 102-patient OrigAMI-4 efficacy population, response rate was 42%. Continued approval requires confirmatory clinical benefit; this is not traditional full approval.

Phillips Medisize / Business Wire

Phillips Medisize acquires full Chippenham site footprint for inhalation development

Phillips Medisize announced an investment to acquire the complete footprint of its Chippenham site in England, strengthening its Global Inhalation Center of Excellence alongside Cambridge. Building on the 2025 Vectura acquisition, the site supports drug-device formulation development and early- and late-stage clinical supplies. The announcement links the investment to anticipated growth in complex inhaled therapies.

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Sources & open questions

  • Available capacity, site-specific qualifications, project delivery history, pricing, and technology transfer terms require confirmation with the execution entity.
  • Company service pages support the stated scope but do not establish clinical validation of every dosage form or client program.
  • The group, subsidiary, and execution site should be confirmed separately before project initiation and contracting. They should not be counted as three independent groups.
  • Public sources confirm service availability. Sample suitability, scope of work, pricing, turnaround time, success criteria, and the quality system require direct confirmation.
  • This record describes service capabilities, not the clinical progress of a drug candidate or an independent validation of service success rates.
  • The website confirms commercial MicroED services. The ED-1 commissioning and acceptance dates, execution site, criteria for absolute configuration assignment, and quality system require direct confirmation.
  • This record covers small molecules and pharmaceutical solid-state analysis. General cryo-EM protein analysis is not treated as evidence of protein MicroED.
  1. First-Time-Right Formulation Development ↗Crystal Pharmatech · Undated; retrieved 2026-11-01
  2. Solid Form Screening ↗Crystal Pharmatech · Undated; retrieved 2026-11-01
  3. Solid Form CRO & Formulation CDMO Services ↗Crystal Pharmatech · Undated; retrieved 2026-11-01
  4. Crystal Pharmatech and ELDICO Dedicated MicroED Platform ↗Crystal Pharmatech · 2026-04-16
  5. Crystal Pharmatech — LinkedIn ↗Crystal Pharmatech · Not stated
  6. Company history: founded in 2010; USD 14.5 million Series B disclosed in 2018; CFS/Candoo group relationships. ↗Crystal Pharmatech · Not stated

Inclusion is not endorsement or partner qualification. Assess company claims, clinical evidence, and project-specific capabilities separately.

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