Nallaram pharma  aims to be an “Employer of Choice: A company that is chosen by its current and future employees,” and we are investing time and energy into various initiatives to reach that goal. We want our employees to feel empowered to shape the future of our organization. To that end, we are building a workplace where diverse teams and individuals can thrive amid a culture of mutual learning and respect. We are committed to creating an environment where all our employees can become peak performers at their jobs and stay both physically and mentally healthy.

Key parts of a pharmaceutical manufacturing working people include:

Specification Management

Manages the specification of the Raw Material (RM), Intermediate Product (IP) and Final Product (FP)

Recipe Management: Defines the components of the product

Batch Management: Manages RM, IP, and FP batches within the manufacturing flow

Batch Genealogy: Defines the relationship between raw materials and final product to trace which batches are used in which products

Manufacturing Sample Management: Defines batch and sample templates (with associated tests) required for testing RM, IP, and FP

Material and Inventory Management: Manages the inventory of physical samples taken as part of the manufacturing process. Also manages inventory of laboratory consumables, reagents, and chemicals

Supplier Management: Manages suppliers of materials including reagents, consumables, and raw materials

Instrument Calibration and Maintenance: Manages instruments and equipment used within the laboratory ensuring only correctly calibrated and maintained instruments are used for testing

Competency and Training Management: Manages staff training records and the ability to restrict tasks and actions to competent staff

Method Management: Manages the methods associated with analytical tests

CAPA: Manages the quality improvement cycle through corrective actions/preventative actions

Skip Lot/Selective Testing: Manages reduced testing based on defined rules (i.e. test every 20 after 5 good tests)

Work Assignment: Assigns analysts and instruments to tests

Runsheet Management: Manages the creation of analytical runsheets that defines sample test order including blanks and duplicates

Instrument Integration: Integrates with analytical instruments to automate the transfer of results to the LIMS

External ERP Interface: Integrates with external enterprise resource planning solutions (such as SAP). Import of inspection plans and inspection lots and the export of the batch usage decision and analytical results

Product Grading: Manages the assignment of a grade to a product once it has been tested

Chain of Custody: Records a full chain of custody for a sample including both location and responsible person

Certificate of Analysis: Manages the generation of Certificates of Analysis (CoA) and Certificates of Conformance (CoC)

Advanced Analytics: Provides useful statistics about the product (conformance and variation), the laboratory (speed and efficiency), as well as suppliers, customers, and raw materials

Stability Testing: To determine the retention of product quality over time, for shelf-life purposes