Hiring: Technical Proposals & Marketing Engineer

Cybernetik Technologies is one stop solution for all your bagging needs. We develop fully automated packing lines for low, medium and high production capacities that deliver precision filling with the highest level of performance and reliability. We provide complete solutions for automated bag filling, conditioning, sealing and quality checking which can be further combined with any palletizing system. The machine comes with a built-in weight set-up and offers high accuracy in the filling process. It uses load cell for weigh-metric filling. The machine uses a screw feeder for accuracy and can fill products by the touch of a button. As hygiene is the heart of food processing, we have considered stainless steel 316 food grade for all contact parts. All systems are in compliance with the national and international standards for food safety and quality. Application Areas Used for filling fine powder, free or non-free flowing things like wheat flour, atta, gram flour, milk powder, curry powder, coffee powder, pharmaceutical powders, pesticide powders, animal feed, pet foods. Features Ease of operation and maintenance PLC-based controller. Load cell for weigh metric filling. Screw feeder for accurate filling. CE and cGMP compliance. Easy interfacing with the palletizing system. Seamless integration to existing systems. Optional Remote monitoring and control. Click to read more about Auto Bagging For more information about the Auto Bagging Machine, Contact us at [email protected]

The worldwide production and consumption of essential oils and perfumes are increasing at rapid speed. The traditional technologies for extraction of essential oil processing are of great significance, but one cannot deny the fact that they do have significant drawbacks compared to the advanced extraction technique like CO2 Supercritical Extraction. Why are traditional methods of extraction not safe? The traditional methods of essential oil extraction are hydro-distillation or solvent extraction. The concern using the traditional methods is the losses of some volatile compounds, low extraction efficiency, degradation of unsaturated compounds through thermal or hydrolytic effects and toxic solvent residue in the extract. Disadvantages of Water and Steam Distillation Due to the low pressure of rising steam, oils of high-boiling range require a higher quantity of steam for vaporization -hence longer hours of distillation. The plant material becomes wet, which slows down distillation as the steam has to vaporize the water to allow it to condense further up the still. Oxygenated components such as phenols tend to dissolve in the still water, so their complete removal by distillation is not possible. As water distillation tends to be a small operation (operated by one or two persons), it takes a long time to accumulate much oil, so good quality oil is often mixed with lousy quality oil. The distillation process is treated as art by local distillers, who rarely try to optimize both oil yield and quality. Water distillation is a slower process than either water and steam distillation or direct steam distillation. What is the alternative solution to overcome solvent residue and toxic solvents? 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 more […]

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 […]