mRNA Synthesis CRO Services

From Discovery to GLP—Optimized Speed, Quality, and Scale

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Enorna simplifies your preclinical development process through our flexible mRNA synthesis services.

Our end-to-end solutions—spanning from sequence design and gene synthesis to in vitro transcription (IVT)—can deliver research-grade mRNA products in as little as 3 weeks, providing robust support for both in vitro and in vivo studies.

Workflow and Advantages
01

Gene Synthesis

(Optional)
02

Plasmid Preparation

03

Plasmid Linearization

04

In Vitro Transcription (IVT)

Why Us
1Technically Superior mRNA

dsRNA controlled to minimize immune activation

Free-to-operate backbone available

Tailored testing packages

2Cost-Efficient without Quality Compromise

Bulk discounts for multi-project deals 

Value-added services – free consultations

3IP Solution Provider

Patent-protected alternatives: Our proprietary caps, enzymes, and LNPs come with clear IP ownership, eliminating legal uncertainties.

Affordable access: Transparent licensing fees, no hidden royalties.

Drop-in replacements: Compatible with industry-standard

4Scalable & Phase-Ready Manufacturing

Seamless scale-up: GLP-grade batches up to 100 mg, GMP-grade CDMO services beyond

Consistent quality: smooth transition from pre-clinical to clinical

mRNA CDMO Solutions
Services

We provide research grade and GLP grade mRNA synthesis services for both in vitro and in vivo studies.

 
Research Grade
GLP Grade
RNA Type
mRNA, saRNA
mRNA, saRNA
Sequence Length*
0-15 kb
0-15 kb
Scale
1-10 mg
20-100 mg
Turnaround Time
7-10 Business Days
10-12 Business Days
Deliverable

a) Individual Cryotubes

b) ROA

a) Individual Cryotubes

b) ROA

*Additional fee may be charged for sequence longer than 7 kb.
Customizable Options
  • 5’ Cap Options

    Co-transcriptional capping:

    • Partner-supplied Cap (Cap 1 structure)

    • AG

    • AG (3' OMe)

    • AU

    • Proprietary AG analog (FTO- guaranteed, licensable IP) 

    Enzymatic capping:Vaccine capping system

  • Modified NTP Options

    •  m1ψ-UTP•  m5C

    •  ψ-UTP•  m6A

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Testing Panel
  • QC
    Item
    Method
    Standard
    Research Grade
    Preclinical Grade
  • Identification
    Appearance
    Visual Inspect
    Clear and free of foreign particles
    RNA length and intergrity
    Agarose Gel Electrophoresis
    Expected size band detected
    Poly A length
    Enzyme digestion to LC-MS
    Target ± 5%
    RNA content
    UV Absorbance
    Target ± 5%
    pH
    pHmeter
    Target ± 0.5
    Buffer Spefication
    Client Spec
    N/A
  • Purity
    A260/280
    UV Spec
    1.70 ~ 2.30
    Capping efficiency
    LC-MS
    ≥ 90%
    Size based purity
    Capillary Electrophoresis

    <4k nt: ≥75%

    >4k nt: report value

  • Impurity
    Total protein residue
    Nano Orange Assay
    ≤1%
    Plasmid DNA residue
    qPCR
    ≤0.05%
    dsRNA
    ELISA
    ≤0.1%
  • Safety
    Endotoxin
    Semiquantitative
    < 10EU/mg
    Bioburden
    Direct inoculation
    No Growth after 72 hrs

Y

N

Optional

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