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Reali Tide Biological Technology Weihai - CDMO/CMO

Reali Tide can provide one-stop CDMO service from R&D to commercial production, especially for advanced intermediates and new compounds with “special high quality ” and “cost saving” requirements after signing non-disclosure agreements.Reali Tide are equipped with various facilities for special chemical reactions and testing conditions, including HPLC, UPLC, GC, GCMS, UV, etc., to provide you various testing services for products throughout the entire product development cycle. We are also a manufacturer of cosmetics ingredients with high quality.We have innovative technologies that enhance the transdermal absorption of ingredients.

Address: East of Longhai Road, North of Binhai Road, Nanhai New District, Weihai City, Shandong Province, , Weihai
China
China Local time:

PFAS-Free Peptides

Certified Quality & Sustainability with ISO 9000 certification and RSPO audited supplier & GMP

Specialized in APIs & Pharmaceutical Intermediates

Our services:

Drug Substance
Drug Product

Production scale:

small
medium
large

Response time:

Employees:
200
Established in:
2016

Upcoming events

CPHI Europe 2025

CPHI Europe 2025

In-person event

28-10-2025

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Services

Drug Substance (CDMO/CRO)

Pharmaceutical intermediates are compounds used in the production of APIs. CDMOs play a crucial role in synthesizing, scaling, and ensuring the quality of these intermediate compounds to support efficient drug manufacturing.
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Oligonucleotides are short DNA or RNA sequences used in genetic medicine, diagnostics, and gene therapy. Specialized CDMOs offer custom synthesis, modification, and GMP manufacturing services for therapeutic oligonucleotides.
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Peptides are short chains of amino acids with therapeutic potential across endocrinology, oncology, and metabolic disorders. CDMOs offer synthesis, purification, and formulation services tailored to peptide APIs and drug products.
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Small molecule APIs form the backbone of many pharmaceutical drugs due to their low molecular weight and ease of synthesis. They are widely used in treating a range of diseases and are typically produced through chemical synthesis in GMP-compliant facilities.
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Drug Product (CMO)

Liquid oral products such as syrups and suspensions are used for pediatric and geriatric patients. CMOs offer formulation, mixing, filling, and packaging solutions for liquid drug products.
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Oral solid dosage forms like tablets and capsules are the most common drug delivery formats. CMOs offer services in formulation, tableting, encapsulation, and packaging under GMP conditions.
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Powders and granules are oral solid formats used in sachets, suspensions, or direct consumption. CMOs offer blending, granulation, and filling services to ensure consistent quality and performance.
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Tablets and capsules are the most widely used oral dosage forms due to their stability and patient compliance. CMOs provide formulation development, compression, encapsulation, and packaging services under GMP standards.
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Sterile injectables require precise manufacturing conditions. CMOs offer aseptic filling, lyophilization, and regulatory support for injectable formulations, including small molecules and biologics.
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Contact Reali Tide Biological Technology (Weihai) Co., Ltd for Contract Services Expertise

Connect with Reali Tide Biological Technology (Weihai) Co., Ltd, a leading pharmaceutical company from China. They offer specialized Drug Substance (CDMO/CRO), Drug Product (CMO), of which the services for CMO/CDMO include Tablets & Capsules, Powders & Granules. Contact Reali Tide Biological Technology (Weihai) Co., Ltd for free and discover if they are the perfect partner for your pharmaceutical needs.

Drug Substance (CDMO/CRO)

Drug Substance CDMOs and CROs provide essential services in the development and manufacturing of active pharmaceutical ingredients (APIs). These organizations specialize in early-stage research, process development, and GMP-compliant manufacturing of drug substances for clinical and commercial use.


Pharmaoffer's Drug Substance CDMO/CRO category includes partners with expertise in small molecules, biologics, peptides, and complex chemistry, all operating under strict regulatory compliance. These providers help companies scale from lab to market efficiently and cost-effectively.


Key Functions of Drug Substance CDMOs/CROs:


  • API Research and Development: Providing early-stage discovery support, custom synthesis, and process optimization to streamline the development of drug substances.

  • Process Scale-Up and Tech Transfer: Transitioning from bench-scale to pilot and commercial scale production with validated methods and reproducibility.

  • GMP Manufacturing: Delivering high-quality API batches in GMP-certified environments, adhering to FDA, EMA, and other international standards.

  • Analytical Services: Offering comprehensive analytical method development and validation to ensure consistent quality and regulatory compliance.

  • Flexible and Specialized Capabilities: From small molecule synthesis to biologic and peptide manufacturing, these partners provide specialized services tailored to product-specific needs.


Explore Leading API CDMOs and CROs

Pharmaoffer connects you with trusted CDMOs and CROs for drug substance development. Our platform enables seamless access to specialized service providers equipped to support your API lifecycle from discovery to commercialization.

Drug Product (CMO)

Drug Product CMOs focus on the manufacturing and packaging of finished pharmaceutical dosage forms. These contract partners provide scalable production solutions that meet global regulatory and quality standards, supporting pharma companies throughout the drug product lifecycle.


Pharmaoffer’s Drug Product CMO category includes providers capable of manufacturing oral solids, injectables, topical formulations, and more—whether for clinical trials or commercial distribution.


Key Functions of Drug Product CMOs:


  • Formulation Development: Supporting the transition from drug substance to drug product through formulation optimization and compatibility testing.

  • Clinical and Commercial Manufacturing: Offering pilot-scale to high-volume manufacturing for various dosage forms under GMP conditions.

  • Packaging and Serialization: Providing primary and secondary packaging with serialization and tamper-proof labeling to meet compliance requirements.

  • Regulatory Support: Ensuring that all production meets FDA, EMA, and ICH standards for drug product quality, safety, and traceability.

  • Flexible Production Lines: Handling diverse dosage forms including tablets, softgels, liquids, and sterile injectables.


Partner with Proven Drug Product CMOs

Through Pharmaoffer, discover CMOs that excel in drug product manufacturing. Whether you need small-scale batches or full commercial output, our platform connects you with the right partners for compliant, cost-effective solutions.

Oral solid products

Oral solid products include tablets and capsules. CMOs provide formulation development, manufacturing, and packaging of solid dosage forms.

Tablets & Capsules

Tablets and capsules are common oral solid forms. CMOs offer formulation, compression, encapsulation, and GMP-compliant manufacturing services.

Powders & Granules

Powders and granules are flexible oral formats. CMOs support blending, granulation, and GMP filling for pharmaceutical applications.

Reali Tide Biological Technology Weihai


Reali Tide can provide one-stop CDMO service from R&D to commercial production, especially for advanced intermediates and new compounds with “special high quality ” and “cost saving” requirements after signing non-disclosure agreements.Reali Tide are equipped with various facilities for special chemical reactions and testing conditions, including HPLC, UPLC, GC, GCMS, UV, etc., to provide you various testing services for products throughout the entire product development cycle. We are also a manufacturer of cosmetics ingredients with high quality.We have innovative technologies that enhance the transdermal absorption of ingredients.