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Why CO2 Extraction ?
05.13.19

Why CO2 Extraction ?

The conventional Extraction process has limitations of solvent toxicity, presence of residual solvents in the final extract and even loss of heat-sensitive oils.

The rapidly emerging Supercritical fluid extraction technology is attracting more global markets and larger profits.

Supercritical CO2 is becoming the preferred extraction choice for the industry.


Top 10 reasons to go for CO2 Extraction

1. USFDA approved “Green Technology”.

2. One Machine– Multiple business solutions.

3. Easy available, Safest – fully Recoverable Media.

4. Higher extraction efficiency, the benefit of Selective Extraction.

5. Operates without altering or damaging products natural properties.

6. No effluent generation and No pollution related hassles & costs.

7. Lower operating costs, Global markets ensuring Higher Profits.

8. 100 % cGMP Compliance, Food & Pharma grade Equipment.

9. Ready Pilot Plant to assist actual business, product and process trials.

10. 30 years old Automation  Company – Proprietary Designs, Project costs reduced by 60%.

Contact

For more details about the CO2 Extraction please do contact at sales.automation@cybernetik.com

21.04.20

Equipment Validation For Pharmaceutical Equipment

Equipment Validation For Pharmaceutical Equipment

How Important is Equipment Validation in the Pharma Industry? Disasters often stir humankind into constructive action. It was in the wake of the infamous “Contergan Scandal” that Good Manufacturing Practice (GMP) evolved in the United States in 1963 [1]. And, the issue of sterility in the parenteral market made two Food and Drug Administration (FDA) officials put forth the concept of validation in 1979 [2]. Pharma products have a direct impact on the health of the consumers. Ensuing quality of products is, therefore, a top priority for regulators. Dosage strongly impacts the percentage of the drug that reaches the site of action. Therefore, each batch of manufactured drugs must be of the same quality [3], meaning consistency is of paramount importance. Equipment Validation documents evidence that a piece of equipment conforms with the required standards across all stages [4]. GMP ensures that quality is an integral part of a product and not merely tested in it [5]. Equipment validation is a component of GMP which guarantees that the equipment maintains the required standards and, as a result, consistently provides products of the necessary quality [5]. Cybernetik Technologies has successfully validated and delivered multiple pieces of equipment for the pharmaceutical industry. Our technicians engage with clients throughout the equipment validation process, while conforming with the US FDA Part 211 and Part 11, EU Annexe 11, and cGMP standards, and also drafting the necessary documents. When the validated equipment is part of a larger process, the validation documents play another key, although indirect, role – that of rapid error detection. If the process output is not as expected, technicians need to pin point the error. They can safely rule out equipment defect because it is already validated [6].   Equipment Validation for Pharma Industry Equipment Cybernetik Technologies implements validation for pharmaceutical equipment […]

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14.09.17

Effectiveness Of Automatic Bagging Systems

Effectiveness Of Automatic Bagging Systems

Industrial Robotics has come a long way since its inception back in the 1960’s. It has now become one of the key elements of competitive manufacturing and production, which helps achieve high productivity, quality and adaptability at minimal costs. Recent advancements and research in automation has helped industrial robots far supersede over Special Purpose Machines (SPM’s) in executing tasks and operations of varied nature across multiple industries.Lets look at some of the fundamental benefits of working

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24.05.18

Innovative Technique in Agro Processing: Supercritical Fluid Extraction (SCFE)

Innovative Technique in Agro Processing: Supercritical Fluid Extraction (SCFE)

Innovations in food processing industry are comparatively slow, as safety and quality are always the primary concerns.

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