PCB Process Flow Multilayer Manufacturing Flowchart

•

9 likes•18,775 views

Flowchart of multilayer bare printed circuit board fabrication process. Flow chart available in poster format.

PCB Process Flow Multilayer Manufacturing Flowchart

Our PCB 101 Presentation goes through the processes involved in manufacturing a printed circuit board. From a simple single sided board to a complex multi-layer, double sided surface mount design, our goal is to provide you a design that meets your requirements and is the most cost effective to manufacture. Our experience in IPC Class III standards, very stringent cleanliness requirements, heavy copper and production tolerances allow us to provide our customers exactly what they need for their end product.

New microsoft power point presentation

Potturi Bhavana

Pcb designing

ADERSH VIMAL

Smt tht pcb design and manufacture

Shenzhen Southern Machinery Sales And Service Co., Ltd

PCB Terminologies in PCB designing

MSHOAIBASLAM1

PCB shweta16797

Surface Mount Technology (SMT) refers to a specific type of electronics assembly where electronic components are attached to the surface of a substrate (typically a printed circuit board). SMT is a modern alternative to traditional thru-hole technology where components are attached to substrates by leads that passed through holes in the PCB. Surface Mount components require less space so SMT is helpful in product miniaturization. SMT Overview SMT V/S THROUGH HOLE Basic SMT process flow Equipments used SMT Assembly Through Hole Assembly & Soldering ELECTROSTATIC DISCHARGE RoHS

Introduction to PCB Designing

Sharan kumar

In Plant training (internship) at Schneider Electric

Sujith Js

Surface mount technologyprernamalhotra

Printed Circuit Board Manufacturing

Richard Puthota

INTRODUCTION TO PCBprasanna kumar

Film interpretation

Gholam reza mohammadi

Printed circuit board(pcb)

Ujjwal Choubey

Pad design and process for voiding control at QFN assemblynclee715

Steps to Compliance with the European Medical Device Regulations

April Bright

The trilogue negotiations for the European Medical Device Regulations are expected to conclude by June. Whether or not the long-awaited regulations receive another postponement, orthopaedic manufacturers cannot put off preparation or they risk their ability to sell products in Europe. Dr. Tariah will walk attendees through the greatest pain points for orthopaedic manufacturers when complying with the new regulations.

Instrument Testing and Validation

April Bright

What's hot

Types of PCB Designing Layers

Sharan kumar

Pcb design powerpoint

Prashant329822

PCB Layout Fundamentals

Analog Devices, Inc.

PCB Production Introduction /How to Make PCB (1)

Agile Circuit Co., Ltd

Printed circuit Board DescriptionRUBY DIKSHIT

Pcb designingBhanu Sharma

Multilayer PCB Manufacturing Process

Richard Houghton

Workshop on pcb

Mahmudur Rana

PCB Designing

kaleem Ullah

Smt basicsPennyTang2012

Double sided PCB manufacturing

Aditya Todi

Introduction to Surface Mount Technology

ABDUL MUNAFF

Introduction to PCB Designing

Sharan kumar

In Plant training (internship) at Schneider Electric

Sujith Js

Surface mount technologyprernamalhotra

Printed Circuit Board Manufacturing

Richard Puthota

INTRODUCTION TO PCBprasanna kumar

Film interpretation

Gholam reza mohammadi

Printed circuit board(pcb)

Ujjwal Choubey

Pad design and process for voiding control at QFN assemblynclee715

What's hot (20)

Types of PCB Designing Layers

Pcb design powerpoint

PCB Layout Fundamentals

PCB Production Introduction /How to Make PCB (1)

Printed circuit Board Description

Pcb designing

Multilayer PCB Manufacturing Process

Workshop on pcb

PCB Designing

Smt basics

Double sided PCB manufacturing

Introduction to Surface Mount Technology

Introduction to PCB Designing

In Plant training (internship) at Schneider Electric

Surface mount technology

Printed Circuit Board Manufacturing

INTRODUCTION TO PCB

Film interpretation

Printed circuit board(pcb)

Pad design and process for voiding control at QFN assembly

Viewers also liked

Steps to Compliance with the European Medical Device Regulations

April Bright

Instrument Testing and Validation

April Bright

SURFACE MOUNT TECHNOLOGYSubhendra Singh

PCBA Assembly Process Flow / PCB Assembly Manufacturing

Agile Circuit Co., Ltd

How to Implement ISO 13485 Updates

April Bright

Significant changes are underway that impact the quality and regulatory systems of medical device companies and their suppliers. ISO 13485:2016 adds new requirements to address risk management and to better align the standard with global regulatory requirements (FDA, MDD, JPAL, etc.). With the release of ISO 9001:2015, the ISO 9001 and ISO 13485 standards are no longer integrated. A new single audit MDSAP program will be in effect beginning 2017 that incorporates applicable FDA, Canadian, Brazilian, Australian and Japanese quality system requirements into the annual ISO 13485 audit cycle. The presentation will provide an overview of these changes and the steps required to incorporate these changes into existing quality management systems.

Strategies for Device Approval in China, India, South Korea and Australia

April Bright

This session will describe the orthopaedic device regulatory and registration requirements in Asia Pacific markets. Regulatory steps and strategies will be presented for each of these countries. The discussion will also cover ways to gain regulatory information about competitors already selling in these markets. Attendees will leave the session with an understanding of timelines, costs and complexity for approval.

Design for Manufacturability Rapid Fire

April Bright

Design for manufacturability (DFM) is a broadly-implemented step in today’s development process to ensure that a designed product can actually be manufactured. While the concept sounds simple, there are nuances to every supplier relationship and every new process. Three suppliers—a contract manufacturer, additive manufacturer and plastics company—will each spend 15 minutes answering the following question: With orthopaedic customers, our greatest DFM pain point is ___ and the best strategy to change that is ___. OEMs will learn best practices and ways to approach DFM with their supplier partners.

ISO 13485:2016 Revisions Webinar

DQS Inc.

SMT

Abhishek Sood

CAPA: Using Risk-Based Decision-Making Toward Closure

April Bright

Implementing a risk‐based CAPA process within a QMS is a necessity in the improvement of controls aligned with product and process non-conformances, adverse events, audit findings, complaints, etc. Making decisions concerning scope and extent about these “defectives” is a modern and cost-saving approach to improvement and compliance. Every non-conformity does not force you to open a corrective action. While almost every problematic issue needs at least a correction, the biggest payback is to use corrective actions on systemically-driven problems that are repetitive and recurring. Applying the methods of determining risk to the device’s complete life cycle will give your company a complete look at all of the device’s risks—including those relative to processes. Manufacturers should be able to justify that they have reduced the risks as far as possible as part of their risk management plan and ongoing corrective and preventive actions.

FDA Focus on Design Controls

April Bright

Design controls are not an easy subject to address during and after the design of medical devices and manufacturing processes. Design controls should drive the device design process, not be an afterthought. This session focuses on treating design as a separate entity within the quality management system, user needs vs. design inputs, continuation of design controls after the transfer process, design review and more.

Surface Mount Technology

SABBULA NAVYA PRAVALIKA

pcb layers in layoutAnum Mairaj

Orthopaedic Device Industry Business Models: 2020 and Beyond

April Bright

During last year’s closing keynote, Dr. Wael Barsoum underscored the importance of producing transformational, innovative products to stay competitive and maintain a strong company and a healthy supply chain. This year, Dr. Bill Tribe will shine the “innovation lens” on the value of transforming your business. Dr. Tribe co-authored the often-cited “Medical Devices: Equipped for the Future?” study in which the orthopaedics sector is called out specifically as facing an extreme combination of forces — none of which come as a surprise or are new, but when viewed holistically (as in the image below), paint a rather obvious picture of the need for companies to respond. As you can see, orthopaedics is the only sector with 4 of 5 “hot” areas…and in this case, the odd one out (regulatory scrutiny) is still marked “critical.” From a top-down view, the five “disruptors” listed above are acute (power shift to payors, regulatory scrutiny, unclear sources of innovation, new healthcare delivery models, need to serve lower socio-economic classes). They impact the overall orthopaedic industry intensely – but how are they impacting you? Dr. Tribe’s Keynote Address will take into account the uniqueness of the OMTEC audience: large and small OEMs, Suppliers and Service Providers. As stated in the A.T. Kearney study, “Each company faces a different set of headwinds…while the macro-factors held true, individual experiences and prioritization depended on factors such as market geography, product life cycles and go-to-market strategies. The most effective strategies are therefore likely to be company specific.” What will be your business model in 2020? 2025? Will you be considering cost-structure, deployment of inventory, commercial logistics, quality and regulatory frameworks, R&D, innovation and data collection? Dr. Tribe will break down the issues and share potential approaches to help you navigate toward a more relevant and lucrative business model – regardless of where you are in the process.

Surface Mount Manufacturing Basics

SIM

Understanding the New ISO 13485:2016 Revision

Greenlight Guru

he much anticipated revision to ISO 13485, the global medical device quality management system (QMS) standard, was released late last month (Feb, 2016). The new ISO 13485:2016 ushers in a whole new wave of changes and requirements medical device manufacturers must adhere to, which we covered on our previous webinar here (http://www.greenlight.guru/webinar/iso-13485-2016-changes). ISO tells us that there will be a three year transition period after which the guidance says, “any existing certification issued to ISO 13485:2003 will not be valid.” The time to start planning your organization's transition to ISO 13485:2016 is now. Or face playing expensive catch up later. (You can view the full webinar here: http://www.greenlight.guru/webinar/iso-13485-2016-transition-planning) In this webinar, you'll learn specifically: What your organization needs to be doing to prepare for the transition to ISO 13485:2016 Why the transition presents an opportunity for your organization to implement better processes An overview of the specific changes coming with ISO 13485:2016 The actions you should be taking now and how to plan for the implementation of the standard

Viewers also liked (16)

Steps to Compliance with the European Medical Device Regulations

Instrument Testing and Validation

SURFACE MOUNT TECHNOLOGY

PCBA Assembly Process Flow / PCB Assembly Manufacturing

How to Implement ISO 13485 Updates

Strategies for Device Approval in China, India, South Korea and Australia

Design for Manufacturability Rapid Fire

ISO 13485:2016 Revisions Webinar

SMT

CAPA: Using Risk-Based Decision-Making Toward Closure

FDA Focus on Design Controls

Surface Mount Technology

pcb layers in layout

Orthopaedic Device Industry Business Models: 2020 and Beyond

Surface Mount Manufacturing Basics

Understanding the New ISO 13485:2016 Revision

Recently uploaded

Kubernetes & AI - Beauty and the Beast !?! @KCD Istanbul 2024

Tobias Schneck

As AI technology is pushing into IT I was wondering myself, as an “infrastructure container kubernetes guy”, how get this fancy AI technology get managed from an infrastructure operational view? Is it possible to apply our lovely cloud native principals as well? What benefit’s both technologies could bring to each other? Let me take this questions and provide you a short journey through existing deployment models and use cases for AI software. On practical examples, we discuss what cloud/on-premise strategy we may need for applying it to our own infrastructure to get it to work from an enterprise perspective. I want to give an overview about infrastructure requirements and technologies, what could be beneficial or limiting your AI use cases in an enterprise environment. An interactive Demo will give you some insides, what approaches I got already working for real.

IOS-PENTESTING-BEGINNERS-PRACTICAL-GUIDE-.pptx

Abida Shariff

When stars align: studies in data quality, knowledge graphs, and machine lear...

Elena Simperl

FIDO Alliance Osaka Seminar: The WebAuthn API and Discoverable Credentials.pdf

FIDO Alliance

The Future of Platform Engineering

Jemma Hussein Allen

GenAISummit 2024 May 28 Sri Ambati Keynote: AGI Belongs to The Community in O...

Sri Ambati

Assuring Contact Center Experiences for Your Customers With ThousandEyes

ThousandEyes

Key Trends Shaping the Future of Infrastructure.pdf

Cheryl Hung

Essentials of Automations: Optimizing FME Workflows with Parameters

Safe Software

Are you looking to streamline your workflows and boost your projects’ efficiency? Do you find yourself searching for ways to add flexibility and control over your FME workflows? If so, you’re in the right place. Join us for an insightful dive into the world of FME parameters, a critical element in optimizing workflow efficiency. This webinar marks the beginning of our three-part “Essentials of Automation” series. This first webinar is designed to equip you with the knowledge and skills to utilize parameters effectively: enhancing the flexibility, maintainability, and user control of your FME projects. Here’s what you’ll gain: - Essentials of FME Parameters: Understand the pivotal role of parameters, including Reader/Writer, Transformer, User, and FME Flow categories. Discover how they are the key to unlocking automation and optimization within your workflows. - Practical Applications in FME Form: Delve into key user parameter types including choice, connections, and file URLs. Allow users to control how a workflow runs, making your workflows more reusable. Learn to import values and deliver the best user experience for your workflows while enhancing accuracy. - Optimization Strategies in FME Flow: Explore the creation and strategic deployment of parameters in FME Flow, including the use of deployment and geometry parameters, to maximize workflow efficiency. - Pro Tips for Success: Gain insights on parameterizing connections and leveraging new features like Conditional Visibility for clarity and simplicity. We’ll wrap up with a glimpse into future webinars, followed by a Q&A session to address your specific questions surrounding this topic. Don’t miss this opportunity to elevate your FME expertise and drive your projects to new heights of efficiency.

GDG Cloud Southlake #33: Boule & Rebala: Effective AppSec in SDLC using Deplo...

James Anderson

Effective Application Security in Software Delivery lifecycle using Deployment Firewall and DBOM The modern software delivery process (or the CI/CD process) includes many tools, distributed teams, open-source code, and cloud platforms. Constant focus on speed to release software to market, along with the traditional slow and manual security checks has caused gaps in continuous security as an important piece in the software supply chain. Today organizations feel more susceptible to external and internal cyber threats due to the vast attack surface in their applications supply chain and the lack of end-to-end governance and risk management. The software team must secure its software delivery process to avoid vulnerability and security breaches. This needs to be achieved with existing tool chains and without extensive rework of the delivery processes. This talk will present strategies and techniques for providing visibility into the true risk of the existing vulnerabilities, preventing the introduction of security issues in the software, resolving vulnerabilities in production environments quickly, and capturing the deployment bill of materials (DBOM). Speakers: Bob Boule Robert Boule is a technology enthusiast with PASSION for technology and making things work along with a knack for helping others understand how things work. He comes with around 20 years of solution engineering experience in application security, software continuous delivery, and SaaS platforms. He is known for his dynamic presentations in CI/CD and application security integrated in software delivery lifecycle. Gopinath Rebala Gopinath Rebala is the CTO of OpsMx, where he has overall responsibility for the machine learning and data processing architectures for Secure Software Delivery. Gopi also has a strong connection with our customers, leading design and architecture for strategic implementations. Gopi is a frequent speaker and well-known leader in continuous delivery and integrating security into software delivery.

De-mystifying Zero to One: Design Informed Techniques for Greenfield Innovati...

Product School

"Impact of front-end architecture on development cost", Viktor Turskyi

Fwdays

I have heard many times that architecture is not important for the front-end. Also, many times I have seen how developers implement features on the front-end just following the standard rules for a framework and think that this is enough to successfully launch the project, and then the project fails. How to prevent this and what approach to choose? I have launched dozens of complex projects and during the talk we will analyze which approaches have worked for me and which have not.

From Siloed Products to Connected Ecosystem: Building a Sustainable and Scala...

Product School

Empowering NextGen Mobility via Large Action Model Infrastructure (LAMI): pav...

Thierry Lestable

ODC, Data Fabric and Architecture User Group

CatarinaPereira64715

From Daily Decisions to Bottom Line: Connecting Product Work to Revenue by VP...

Product School

Connector Corner: Automate dynamic content and events by pushing a button

DianaGray10

Here is something new! In our next Connector Corner webinar, we will demonstrate how you can use a single workflow to: Create a campaign using Mailchimp with merge tags/fields Send an interactive Slack channel message (using buttons) Have the message received by managers and peers along with a test email for review But there’s more: In a second workflow supporting the same use case, you’ll see: Your campaign sent to target colleagues for approval If the “Approve” button is clicked, a Jira/Zendesk ticket is created for the marketing design team But—if the “Reject” button is pushed, colleagues will be alerted via Slack message Join us to learn more about this new, human-in-the-loop capability, brought to you by Integration Service connectors. And... Speakers: Akshay Agnihotri, Product Manager Charlie Greenberg, Host

Slack (or Teams) Automation for Bonterra Impact Management (fka Social Soluti...

Jeffrey Haguewood

Sidekick Solutions uses Bonterra Impact Management (fka Social Solutions Apricot) and automation solutions to integrate data for business workflows. We believe integration and automation are essential to user experience and the promise of efficient work through technology. Automation is the critical ingredient to realizing that full vision. We develop integration products and services for Bonterra Case Management software to support the deployment of automations for a variety of use cases. This video focuses on the notifications, alerts, and approval requests using Slack for Bonterra Impact Management. The solutions covered in this webinar can also be deployed for Microsoft Teams. Interested in deploying notification automations for Bonterra Impact Management? Contact us at sales@sidekicksolutionsllc.com to discuss next steps.

Search and Society: Reimagining Information Access for Radical Futures

Bhaskar Mitra

The field of Information retrieval (IR) is currently undergoing a transformative shift, at least partly due to the emerging applications of generative AI to information access. In this talk, we will deliberate on the sociotechnical implications of generative AI for information access. We will argue that there is both a critical necessity and an exciting opportunity for the IR community to re-center our research agendas on societal needs while dismantling the artificial separation between the work on fairness, accountability, transparency, and ethics in IR and the rest of IR research. Instead of adopting a reactionary strategy of trying to mitigate potential social harms from emerging technologies, the community should aim to proactively set the research agenda for the kinds of systems we should build inspired by diverse explicitly stated sociotechnical imaginaries. The sociotechnical imaginaries that underpin the design and development of information access technologies needs to be explicitly articulated, and we need to develop theories of change in context of these diverse perspectives. Our guiding future imaginaries must be informed by other academic fields, such as democratic theory and critical theory, and should be co-developed with social science scholars, legal scholars, civil rights and social justice activists, and artists, among others.

JMeter webinar - integration with InfluxDB and Grafana

RTTS

Watch this recorded webinar about real-time monitoring of application performance. See how to integrate Apache JMeter, the open-source leader in performance testing, with InfluxDB, the open-source time-series database, and Grafana, the open-source analytics and visualization application. In this webinar, we will review the benefits of leveraging InfluxDB and Grafana when executing load tests and demonstrate how these tools are used to visualize performance metrics. Length: 30 minutes Session Overview ------------------------------------------- During this webinar, we will cover the following topics while demonstrating the integrations of JMeter, InfluxDB and Grafana: - What out-of-the-box solutions are available for real-time monitoring JMeter tests? - What are the benefits of integrating InfluxDB and Grafana into the load testing stack? - Which features are provided by Grafana? - Demonstration of InfluxDB and Grafana using a practice web application To view the webinar recording, go to: https://www.rttsweb.com/jmeter-integration-webinar

Recently uploaded (20)

Kubernetes & AI - Beauty and the Beast !?! @KCD Istanbul 2024

IOS-PENTESTING-BEGINNERS-PRACTICAL-GUIDE-.pptx

When stars align: studies in data quality, knowledge graphs, and machine lear...

FIDO Alliance Osaka Seminar: The WebAuthn API and Discoverable Credentials.pdf

The Future of Platform Engineering

GenAISummit 2024 May 28 Sri Ambati Keynote: AGI Belongs to The Community in O...

Assuring Contact Center Experiences for Your Customers With ThousandEyes

Key Trends Shaping the Future of Infrastructure.pdf

Essentials of Automations: Optimizing FME Workflows with Parameters

GDG Cloud Southlake #33: Boule & Rebala: Effective AppSec in SDLC using Deplo...

De-mystifying Zero to One: Design Informed Techniques for Greenfield Innovati...

"Impact of front-end architecture on development cost", Viktor Turskyi

From Siloed Products to Connected Ecosystem: Building a Sustainable and Scala...

Empowering NextGen Mobility via Large Action Model Infrastructure (LAMI): pav...

ODC, Data Fabric and Architecture User Group

From Daily Decisions to Bottom Line: Connecting Product Work to Revenue by VP...

Connector Corner: Automate dynamic content and events by pushing a button

Slack (or Teams) Automation for Bonterra Impact Management (fka Social Soluti...

Search and Society: Reimagining Information Access for Radical Futures

JMeter webinar - integration with InfluxDB and Grafana

PCB Process Flow Multilayer Manufacturing Flowchart

Recommended

Recommended

More Related Content

What's hot

What's hot (20)

Viewers also liked

Viewers also liked (16)

More from Domestic PCB Fabrication

More from Domestic PCB Fabrication (20)

Recently uploaded

Recently uploaded (20)